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61. 1992 International Fragile X Conference
$160.00
62. Angina Pectoris with Normal Coronary
 
$151.61
63. Fragile Sites on Human Chromosomes
 
$419.49
64. Genome Maps & Neurological
 
$5.95
65. New fragile X often misdiagnosed
$7.95
66. Fragile X mental retardation protein
 
$9.95
67. Limiting damage: fragile X symptoms
 
$5.95
68. New fragile X condition affects
 
$9.95
69. Flawed stem cells yield fragile
 
$5.95
70. Haplotype study of intermediate-length
$0.01
71. Spelling Love with an X: A Mother,
 
$2.95
72. Alpha-thalassemia X-linked mental
 
$3.45
73. X-linked mental retardation: An
 
$1.95
74. Renpenning syndrome: An entry
 
$2.45
75. FG syndrome: An entry from Thomson
 
$1.95
76. Smith-Fineman-Myers syndrome:
 
$9.95
77. FMR1 premutation linked with ovarian
 
$9.95
78. Premature ovarian failure.(GENETICS
$6.95
79. A Doctor's Guide to Weight Control
 
$5.95
80. Options given for ADHD treatment:

61. 1992 International Fragile X Conference proceedings
 Unknown Binding: 415 Pages (1992)

Isbn: 0915667223
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62. Angina Pectoris with Normal Coronary Arteries: Syndrome X (Developments in Cardiovascular Medicine)
Hardcover: 308 Pages (1994-03-31)
list price: US$330.00 -- used & new: US$160.00
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Asin: 0792326512
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Product Description
Angina pectoris with normal coronary arteriograms is a commonentity which has puzzled cardiologists almost since the advent ofcoronary arteriography. Despite major advances in the understanding ofthe pathophysiology of angina in recent years and a multitude ofstudies on the subject, the cause and mechanisms underlying thesyndrome of angina with normal coronary arteries remain unknown.Indeed, results of investigations are controversial and speculationstill prevails regarding the nature of the so called `Syndrome X'.Almost every important aspect of Syndrome X has been tackled in thebook and the reader is exposed not only to the cardiologists' opinion,but also to the authoritative views of the gastroenterologists,gynaecologists and psychiatrists, extremely well represented in thismonograph. The book deals with `cardiologists' Syndrome X' and not themetabolic entity termed `Syndrome X'. The possible connection betweenthe two, however, is discussed. Angina with Normal Coronary Arteries: Syndrome X contributes tothe understanding of Syndrome X and helps clinicians manage theirSyndrome X-patients better and investigators to open new avenues forresearch. ... Read more


63. Fragile Sites on Human Chromosomes (Oxford Monographs on Medical Genetics)
by Grant R. Sutherland, Frederick Hecht
 Hardcover: 286 Pages (1985-05-02)
list price: US$49.95 -- used & new: US$151.61
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Asin: 0195035429
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Fragile sites--points where chromosomes are apt to break--came to prominence in the late 1970s and are now the subject of much clinical concern and laboratory investigation. They are known or suspected agents in the genesis of mental retardation, birth defects, and cancer. This book, the first to deal with fragile sites on human chromosomes, takes a broad interdisciplinary approach to the subject, incorporating findings from cytogenetics, medical and clinical genetics, population genetics, mental retardation, dysmorphology, and oncology.The book has three interrelated sections.The first, focusing on the laboratory, presents what is known about fragile sites, their cytogenetics, and the conditions of cell culture needed to demonstrate them.A clinical section follows, covering X-linked forms of mental retardation, the clinical features associated with the fragile X, and genetic counseling with fragile sites.The final section considers fragile sites as they relate to genetics, including the possible relationship of fragile sites to cancer and to constitutional chromosome abnormalities.This book contains much previously unpublished material and will be an important resource for geneticists and cytogeneticists, molecular and cancer biologists, oncologists, pediatricians, and other health professionals. ... Read more


64. Genome Maps & Neurological Disorders (Genome Analysis Series; Vol. 6)
 Hardcover: 125 Pages (1993-08)
list price: US$25.00 -- used & new: US$419.49
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Asin: 0879693878
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65. New fragile X often misdiagnosed as Parkinson's.(Across Specialties): An article from: Clinical Psychiatry News
by Timothy F. Kirn
 Digital: 3 Pages (2004-03-01)
list price: US$5.95 -- used & new: US$5.95
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Asin: B00082CS46
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Product Description
This digital document is an article from Clinical Psychiatry News, published by International Medical News Group on March 1, 2004. The length of the article is 670 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: New fragile X often misdiagnosed as Parkinson's.(Across Specialties)
Author: Timothy F. Kirn
Publication: Clinical Psychiatry News (Magazine/Journal)
Date: March 1, 2004
Publisher: International Medical News Group
Volume: 32Issue: 3Page: 84(1)

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66. Fragile X mental retardation protein levels increase following complex environment exposure in rat brain regions undergoing active synaptogenesis [An article from: Neurobiology of Learning and Memory]
by S.A. Irwin, C.A. Christmon, A.W. Grossman, Galvez
Digital: Pages (2005-05-01)
list price: US$7.95 -- used & new: US$7.95
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Asin: B000RR4DVS
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This digital document is a journal article from Neurobiology of Learning and Memory, published by Elsevier in 2005. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Fragile X mental retardation protein (FMRP), which is absent in fragile X syndrome, is synthesized in vitro in response to neurotransmitter activation. Humans and mice lacking FMRP exhibit abnormal dendritic spine development, suggesting that this protein plays an important role in synaptic plasticity. Previously, our laboratory demonstrated increased FMRP immunoreactivity in visual cortex of rats exposed to complex environments (EC) and in motor cortex of rats trained on motor-skill tasks compared with animals reared individually in standard laboratory housing (IC). Here, we use immunohistochemistry to extend those findings by investigating FMRP levels in visual cortex and hippocampal dentate gyrus of animals exposed to EC or IC. Rats exposed to EC for 20 days exhibited increased FMRP immunoreactivity in visual cortex compared with animals housed in standard laboratory caging. In the dentate gyrus, animals exposed to EC for 20 days had higher FMRP levels than animals exposed to EC for 5 or 10 days. In light of possible antibody crossreactivity with closely related proteins FXR1P and FXR2P, FMRP immunoreactivity in the posterior-dorsal one-third of cerebral cortex was also examined by Western blotting following 20 days of EC exposure. FMRP levels were greater in EC animals, whereas levels of FXR1P and FXR2P were unaffected by experience. These results provide further evidence for behaviorally induced alteration of FMRP expression in contrast to its homologues, extend previous findings suggesting regulation of its expression by synaptic activity, and support the theories associating FMRP expression with alteration of synaptic structure both in development and later in the life-cycle. ... Read more


67. Limiting damage: fragile X symptoms modulated in mice.(This Week): An article from: Science News
by P. Barry
 Digital: 2 Pages (2007-12-22)
list price: US$9.95 -- used & new: US$9.95
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Asin: B0012DH75A
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Product Description
This digital document is an article from Science News, published by Thomson Gale on December 22, 2007. The length of the article is 515 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: Limiting damage: fragile X symptoms modulated in mice.(This Week)
Author: P. Barry
Publication: Science News (Magazine/Journal)
Date: December 22, 2007
Publisher: Thomson Gale
Volume: 172Issue: 25-26Page: 387(2)

Distributed by Thomson Gale ... Read more


68. New fragile X condition affects males over age 50: develops a pseudo-Parkinson's disease.(Clinical Rounds): An article from: Family Practice News
by Timothy F. Kirn
 Digital: 3 Pages (2004-03-01)
list price: US$5.95 -- used & new: US$5.95
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Asin: B00082BKNQ
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Editorial Review

Product Description
This digital document is an article from Family Practice News, published by International Medical News Group on March 1, 2004. The length of the article is 684 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: New fragile X condition affects males over age 50: develops a pseudo-Parkinson's disease.(Clinical Rounds)
Author: Timothy F. Kirn
Publication: Family Practice News (Magazine/Journal)
Date: March 1, 2004
Publisher: International Medical News Group
Volume: 34Issue: 5Page: 50(1)

Distributed by Thomson Gale ... Read more


69. Flawed stem cells yield fragile X clues: researchers study genetic disorder via discarded embryos.(SCIENCE NEWS This Week): An article from: Science News
by B. Vastag
 Digital: 2 Pages (2007-11-17)
list price: US$9.95 -- used & new: US$9.95
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Asin: B001167SP2
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Product Description
This digital document is an article from Science News, published by Thomson Gale on November 17, 2007. The length of the article is 512 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: Flawed stem cells yield fragile X clues: researchers study genetic disorder via discarded embryos.(SCIENCE NEWS This Week)
Author: B. Vastag
Publication: Science News (Magazine/Journal)
Date: November 17, 2007
Publisher: Thomson Gale
Volume: 172Issue: 20Page: 310(1)

Distributed by Thomson Gale ... Read more


70. Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size ... alleles.: An article from: Human Biology
by Yvette Curlis, Cuiling Zhang, Jeanette J.A. Holden, Ken Kirkby, Danuta Loesch, R. John Mitchell
 Digital: 23 Pages (2005-02-01)
list price: US$5.95 -- used & new: US$5.95
(price subject to change: see help)
Asin: B000AMCPUQ
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Editorial Review

Product Description
This digital document is an article from Human Biology, published by Thomson Gale on February 1, 2005. The length of the article is 6862 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: KEY WORDS: FRAGILE X DYNAMIC MUTATION, CGG REPEAT, FMR1 GENE, INTERMEDIATE-LENGTH ALLELES, DXS548, FRAXAC1, ATL1, FMRb, HAPLOTYPE ASSOCIATIONS.

Citation Details
Title: Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size FMR1 alleles.
Author: Yvette Curlis
Publication: Human Biology (Magazine/Journal)
Date: February 1, 2005
Publisher: Thomson Gale
Volume: 77Issue: 1Page: 137(15)

Distributed by Thomson Gale ... Read more


71. Spelling Love with an X: A Mother, a Son, and the Gene That Binds Them
by Clare Dunsford
Hardcover: 240 Pages (2007-09-04)
list price: US$24.95 -- used & new: US$0.01
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Asin: 0807072796
Average Customer Review: 4.5 out of 5 stars
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Product Description

A medical memoir and poetic meditation on raising a child with a genetic disorder

Clare Dunsford is the mother of a twenty-one-yearold son with Fragile X syndrome, the most common inherited cause of mental retardation. Spelling Love with an X is the first literary memoir about living with Fragile X, which affects the lives of over a million people in the U.S., including those with the full mutation, their families, and treatment professionals.

When her son was first diagnosed, at age seven, Dunsford received the devastating news that she and three of her four siblings carry the Fragile X premutation and had therefore unknowingly passed on the full mutation to several of their children. An English professor by training, Dunsford draws on classic poetry to explore her new identity as a genetically “flawed” individual and reflect on her life with J.P., a colorful young man with great verbal dexterity and a lovably cheeky streak. “My instinct to find order and consolation in literature,” she writes, “lends a distinct voice to the story of my family’s DNA.” Brimming with warmth and intelligence, Spelling Love with an X shares the disarming insights of a compassionate scholar on motherhood, literature, and genetic inheritance.

"Part poetry, part scientific inquiry, this wonderful memoir is, above all, the story of being complexly human in a world filled with fragility and strength, shadow and light. Clare Dunsford navigates the X that has mapped her own and her son's paths with humor, honesty, and clear-sighted intelligence—and in prose that sings."—Elizabeth Graver, author of The Honey Thief and Awake

“Clare Dunsford does much more than inform us concerning a disorder we know too little about. Through a prose both lucid and beautiful, she is able to communicate the strangeness, even the poetry, of fragile X.” —Clara Claiborne Park, author of The Siege: A Family’s Journey into the World of an Autistic Child and Exiting Nirvana: A Daughter’s Life with Autism

"Spelling Love with an X is a beautifully written journey of a woman toward understanding—of herself, her son, and the twists of fate and DNA that bind them and all of us. Clare Dunsford's powerful and moving memoir is rich with humor, poetry and, most of all, love." —Mitchell Zuckoff, author of Choosing Naia: A Family’s Journey

... Read more

Customer Reviews (10)

1-0 out of 5 stars Not recommended to parents with newly diagnosed children with Fragile X
I downloaded this book to my iPhone Kindle app months after my son's Fragile X diagnosis.The emotional theme of this book is extremely depressing with very little hope, I wish I had never read it as it threw me into a deep depression that took a long time rebound from.I feel that the author is depressed and it shown clearly through her subjective lens of raising her son with Fragile X.DO NOT READ if you have just had a diagnosis!Depression for parents after their children's FX diagnosis is very normal and for me and my wife it was devastating, this book was like being hit in the head with a hammer after I had already been knocked out.

My wife and I are doing better and are working diligently to raise our son with positive feelings, happiness, focusing on the good things, being thankful for what we have, and enjoying the simple things in life.This book does nothing to help you in any of these positive ways.

5-0 out of 5 stars A Classic Love Story
While informing us about Fragile X Syndrome, Clare Dunsford reminds us in a distinctive voice that much more than genes binds us.Her well-told tale captures the complexity of competing realities running through most of our lives -- identity, vocation, family, faith, parenthood (and the profound difference between motherhood and fatherhood), friendship, support, loneliness and love.So we laugh, cry and rejoice with her as she recounts the frustrations and surprises of her childhood, romances, career and parenting experiences. Her references to classic literature make manifest the mystery encountered in human differences no matter the time or culture, a mystery best understood in the binding of body and spirit despite the fragility of either."Spelling Love With an X" is a classic love story.Dunsford's X is her and her family's cross (a cross that marks others' lives in other ways) and is only made bearable in anyone's life by Love which is more Divine than human.Her story offers hope to all of us who want to live and love well.

5-0 out of 5 stars A Mother's Story Told with Great Courage
As a parent of a son with Fragile X who is a couple of years younger than Ms. Dunsford's son, J.P., we've experienced the despair as well as the joy she writes of. Her story is beautifully written and shines with the love we have and hope we need for the future for our adult children. She is able to describe the charming, witty character of her son in a way that rings true for parents ofchildren with Fragile X. It's her own story as well. Life as a carrier of Fragile X has its own challenges - ones you might believe are your own character faults - until you find out, at whatever age, that you are a carrier and that the personal battles you've fought for so long are the result of a genetic defect you were born with. The science is helpful. The research is hopeful. Parents, family, carriers, friends should read this book to get a good look at life with Fragile X.

5-0 out of 5 stars Every Parent and Child
This book is still with me. Those are the best kinds of books, I think, the ones that you remember well after reading them. I think it's because "Spelling Love With An X" resonates beyond its specific circumstances. It's not just about Clare Dunsford and her son, but in some way every parent and child. Or, really, every relationship. As Dunsford wonders aloud at one point in the book, since her family carries the gene, is it possible this or that relatives slight eccentricity is really just an extremely mild manifestation of Fragile X. In other words, most brain disorders are merely exaggerations of characteristics we all understand to some degree. We are all on a spectrum of varying consciousness and need. As a result, Dunsford's exploration of the extreme challenges she faces with her son are more than just a faceless "case study." They do what literature should do at its best. They make her and her son's situation universal.

5-0 out of 5 stars Touching and Intelligent
Clare Dunsford's book is an unusual blend of personal memoir and scientifically researched information drawn from a mother's poignant journey raising a child with Fragile X.Dunsford's book blends poetic elegance with important up to date information about her son's genetic condition,a useful read for anyone living or working with children or adults with any developmental disorder. As a special educator who is also an avid reader I was fascinated. Further, I learned of the relationship that this disorder may have to autism which has touched my extended family and of the hope that the future of medical research holds for all those affected by developmental conditions. Ms Dunsford tells her story with strong emotion and wonderfully crafted writing but does not stray from her goal of sharing the knowledge base she has been accumulating over the 21 years of her charming and interesting son's life. ... Read more


72. Alpha-thalassemia X-linked mental retardation syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Mary, MS, CGC Freivogel
 Digital: 4 Pages (2005)
list price: US$2.95 -- used & new: US$2.95
(price subject to change: see help)
Asin: B000M5B09I
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Editorial Review

Product Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come by—until now. The “Gale Encyclopedia of Genetic Disorders” addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the “Gale Encyclopedia of Genetic Disorders” for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

... Read more

73. X-linked mental retardation: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Chitra, MBBS, MD Venkatasubramanian
 Digital: 5 Pages (2005)
list price: US$3.45 -- used & new: US$3.45
(price subject to change: see help)
Asin: B000M5B3FE
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Editorial Review

Product Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come by—until now. The “Gale Encyclopedia of Genetic Disorders” addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the “Gale Encyclopedia of Genetic Disorders” for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

... Read more

74. Renpenning syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Charles, PhD Schwartz
 Digital: 3 Pages (2005)
list price: US$1.95 -- used & new: US$1.95
(price subject to change: see help)
Asin: B000M5B2S2
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Editorial Review

Product Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come by—until now. The “Gale Encyclopedia of Genetic Disorders” addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the “Gale Encyclopedia of Genetic Disorders” for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

... Read more

75. FG syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Dawn, MS, CGC Jacob
 Digital: 2 Pages (2005)
list price: US$2.45 -- used & new: US$2.45
(price subject to change: see help)
Asin: B000M5B174
Canada | United Kingdom | Germany | France | Japan
Editorial Review

Product Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come by—until now. The “Gale Encyclopedia of Genetic Disorders” addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the “Gale Encyclopedia of Genetic Disorders” for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

... Read more

76. Smith-Fineman-Myers syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i>
by Judy, MS Hawkins
 Digital: 3 Pages (2005)
list price: US$1.95 -- used & new: US$1.95
(price subject to change: see help)
Asin: B000M5B30Y
Canada | United Kingdom | Germany | France | Japan
Editorial Review

Product Description

Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come by—until now. The “Gale Encyclopedia of Genetic Disorders” addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the “Gale Encyclopedia of Genetic Disorders” for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

... Read more

77. FMR1 premutation linked with ovarian failure.(Women's Health): An article from: Internal Medicine News
by Mary Ellen Schneider
 Digital: 3 Pages (2007-08-15)
list price: US$9.95 -- used & new: US$9.95
(price subject to change: see help)
Asin: B00122H2RE
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Product Description
This digital document is an article from Internal Medicine News, published by Thomson Gale on August 15, 2007. The length of the article is 637 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: FMR1 premutation linked with ovarian failure.(Women's Health)
Author: Mary Ellen Schneider
Publication: Internal Medicine News (Magazine/Journal)
Date: August 15, 2007
Publisher: Thomson Gale
Volume: 40Issue: 16Page: 13(1)

Distributed by Thomson Gale ... Read more


78. Premature ovarian failure.(GENETICS IN YOUR PRACTICE)(Clinical report): An article from: Internal Medicine News
by Howard P. Levy
 Digital: 3 Pages (2009-10-01)
list price: US$9.95 -- used & new: US$9.95
(price subject to change: see help)
Asin: B002US7H7Y
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Product Description
This digital document is an article from Internal Medicine News, published by International Medical News Group on October 1, 2009. The length of the article is 777 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available immediately after purchase. You can view it with any web browser.

Citation Details
Title: Premature ovarian failure.(GENETICS IN YOUR PRACTICE)(Clinical report)
Author: Howard P. Levy
Publication: Internal Medicine News (Magazine/Journal)
Date: October 1, 2009
Publisher: International Medical News Group
Volume: 42Issue: 17Page: 47(1)

Article Type: Clinical report

Distributed by Gale, a part of Cengage Learning ... Read more


79. A Doctor's Guide to Weight Control
Mass Market Paperback: 291 Pages (1998-06-01)
list price: US$8.95 -- used & new: US$6.95
(price subject to change: see help)
Asin: 0966407008
Average Customer Review: 1.0 out of 5 stars
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Customer Reviews (1)

1-0 out of 5 stars Has anyone READ this book????
????I am on a low-carb diet -I am looking for good info/recipies/etc. and don't know if I should bother with reading this or not??? ... Read more


80. Options given for ADHD treatment: diagnosable causes.(Children's Health)(Attention Deficit Hyperactivity Disorder): An article from: Family Practice News
by Ben Van Houten
 Digital: 2 Pages (2004-03-01)
list price: US$5.95 -- used & new: US$5.95
(price subject to change: see help)
Asin: B00082BL58
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Editorial Review

Product Description
This digital document is an article from Family Practice News, published by International Medical News Group on March 1, 2004. The length of the article is 362 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: Options given for ADHD treatment: diagnosable causes.(Children's Health)(Attention Deficit Hyperactivity Disorder)
Author: Ben Van Houten
Publication: Family Practice News (Magazine/Journal)
Date: March 1, 2004
Publisher: International Medical News Group
Volume: 34Issue: 5Page: 111(1)

Distributed by Thomson Gale ... Read more


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