61. Search By Disease 2 waardenburg syndrome type I ( WS1). 3 waardenburg syndrome variant. 4 Waardenburgsyndrome with upper limb anomalies. 6 waardenburg syndrome, type III (WS3). http://www.eddnal.com/directory/disease.php?letter=W

62. Health Library - Waardenburg Syndrome Your Health. Search. waardenburg syndrome. Synonyms waardenburg syndromeis a genetic disorder that may be evident at birth (congenital). The http://yourhealth.stlukesonline.org/Library/HealthGuide/IllnessConditions/topic.

63. Healthfinder® — Waardenburg Syndrome waardenburg syndrome. internet URL. description. This fact sheet describesthe causes and types of waardenburg syndrome. related topics. http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=6703&lang=1

64. Health Library - Waardenburg Syndrome Advanced Search. waardenburg syndrome. Synonyms waardenburg syndrome isa genetic disorder that may be evident at birth (congenital). The http://www.stjudemedicalcenter.org/library/healthguide/IllnessConditions/topic.a

65. CCR Research Directory Keyword Search Results Waardenburg Syndrome of Research...... CCR Home Directory Main Page Staff Index Branch Index Keyword IndexResults for Keyword waardenburg syndrome Short http://www-dcs.nci.nih.gov/resdir/find_kw.cfm?kw_id=1740

66. 1Up Health > Waardenberg Syndrome > Causes, Incidence, And Risk Factors Of Waard waardenburg syndrome (WS) . Read detailed information about WaardenburgSyndrome (WS) . Includes a set of questions and answers http://www.1uphealth.com/medical/disease/birth-defects-genetic-disease/waardenbu

1Up Health Waardenberg syndrome Alternative Medicine Clinical Trials ... Health Topics A-Z Search 1Up Health Waardenberg syndrome Information Waardenberg syndrome Causes, Incidence, and Risk Factors Alternative names : Type 3 = Klein-Waardenberg syndrome, Type 4 = Waardenburg-Shah syndrome, Waardenberg syndrome types 1-4 Definition : A group of heritable conditions, which include deafness and partial albinism (pale skin, hair and eye color) as their most important features. Causes, Incidence, and Risk Factors Waardenberg syndrome is inherited as an autosomal dominant trait; only one parent has to pass on the gene for a child to be affected. The multiple types of this syndrome result from mutations occurring in different genes. All types share two dominant features: hearing loss and partial albinism . The albinism is incomplete and may appear as a white forelock in an otherwise dark head of hair, very pale light blue eyes, or two different colored eyes heterochromia ). Other findings that may be seen include wide separation of the inner corners of the eyes with a broad nasal bridge and other pigmentary changes of the skin. Waardenburg syndrome affects about 1 in 30,000 people. Almost 90% of patients have an affected parent but the manifestations of the condition in the parent can be quite different from those in the child.

67. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders Conditions and Diseases Genetic Disorders waardenburg syndrome .Uncover resources and links to Web sites related to Conditions http://www.1uphealth.com/links/genetic-disorders-waardenburg-syndrome.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Genetic Disorders : Waardenburg Syndrome Description See Related Categories Health: Conditions and Diseases: Rare Disorders Sites Human Gene Map An article about Waardenburg syndrome and its features, statistics and the gene pax3. National Library of Medicine Offers synonyms, a summary and a list of major features. NORD - Waardenburg Syndrome A general discussion about this disorder, followed by further resources. Pediatric Database A definition of Waardenburg syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites.

68. Gallaudet University's Genetics Program waardenburg syndrome NIDCD Health Information waardenburg syndrome. Boys TownNational Research Hospital waardenburg syndrome. NCBI waardenburg syndrome. http://depts.gallaudet.edu/genetics/resources1.htm

Home Genetics Clinic Summer Programs in Genetics Studies in Genetic Deafness ... Contact Genetics Program Department of Biology General Genetic Deafness Resources Alexander Graham Bell Association for the Deaf and Hard of Hearing Genetics and Deafness - Ten Syndromes Most Commonly Associated with Hearing Impairment March of Dimes Birth Defects Foundation National Institute on Deafness and Other Communication Disorders (NIDCD) ... Facts on Infant Hearing Loss Blindness and Deafness Resources DB-Link (National Information Clearinghouse on Children who are Deaf-Blind) Deaf-Blind Perspectives Helen Keller National Center for Deaf-Blind Youth and Adults (HKNC) The Foundation Fighting Blindness Connexin deafness National Center for Biotechnology Information (NCBI): Connexin 26 Alport syndrome Alport syndrome Ask NOAH About: Kidney and Urologic Diseases eMedicine: Alport syndrome MEDLINEplus Medical Encyclopedia: Alport syndrome ... National Organization for Rare Disorders Brachio-oto-renal (BOR) syndrome Boys Town National Research Hospital: BOR syndrome Jervell and Lange-Nielsen syndrome (Long-QT syndrome) NCBI: Long-QT syndrome Pendred syndrome What is Pendred Syndrome?: MedicineNet

69. Page Not Found waardenburg syndrome, type I. Syndrome, waardenburg syndrome, type I. Gene Name,Paired box homeotic gene3. Gene Symbol, PAX3. OMIM Number of the Gene, 193500. http://www.nidr.nih.gov/cranio/detail/193500.htm

Please check to see if you entered the correct URL. If you did, it might be that the link no longer exists. As an option, you may do a search of our site. If all else fails, please fill in the form below and send it to the webmaster to report the broken link. Your Name: Email Address: Please indicate the broken URL here: Your browser doesn't support JavaScript. It will, however, affect only two minor things: it will distort the page appearance and will disable the "printer-friendly version" link. NIDCR Home Page Contact us Accessibility Privacy statement ... Search Image in banner: magnified fluoride crystal National Institute of Dental and Craniofacial Research National Institutes of Health Bethesda, MD 20892-2190 e-mail: nidcrinfo@mail.nih.gov phone: 301/496-4261 National Institutes of Health Department of Health and Human Services

70. Page Not Found waardenburg syndrome, type IIA. Syndrome, waardenburg syndrome, type IIA.Gene Name, Microphthalmiaassociated transcription factor. Gene Symbol, MITF. http://www.nidr.nih.gov/cranio/detail/193510.htm

Please check to see if you entered the correct URL. If you did, it might be that the link no longer exists. As an option, you may do a search of our site. If all else fails, please fill in the form below and send it to the webmaster to report the broken link. Your Name: Email Address: Please indicate the broken URL here: Your browser doesn't support JavaScript. It will, however, affect only two minor things: it will distort the page appearance and will disable the "printer-friendly version" link. NIDCR Home Page Contact us Accessibility Privacy statement ... Search Image in banner: magnified fluoride crystal National Institute of Dental and Craniofacial Research National Institutes of Health Bethesda, MD 20892-2190 e-mail: nidcrinfo@mail.nih.gov phone: 301/496-4261 National Institutes of Health Department of Health and Human Services

71. Searchalot Directory For Waardenburg Syndrome Pediatric Database A definition of waardenburg syndrome followed by the epidemiology,pathogenesis, clinical features, investigations and management. http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Waar

Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Genetic Disorders : Waardenburg Syndrome Related Web Sites Pediatric Database - A definition of Waardenburg syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. NORD - Waardenburg Syndrome - A general discussion about this disorder, followed by further resources. Human Gene Map - An article about Waardenburg syndrome and its features, statistics and the gene pax3. National Library of Medicine - Offers synonyms, a summary and a list of major features. Related Categories Health: Conditions and Diseases: Rare Disorders All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut

72. Waardenburg Syndrome Information And Links Click Here KeyWorlds.com Health_Beauty_Fitness Disease WaardenburgSyndrome Links NORD waardenburg syndrome Syndromic Hearing http://www.keyworlds.com/w/waardenburg_syndrome.htm

FREE Game Downloads Today's Featured Game FREE Download - Click Here FREE Download - Click Here FREE Download - Click Here ... Disease : Waardenburg Syndrome Links NORD - Waardenburg Syndrome Syndromic Hearing Loss Waardenburg Syndrome Waardenburg Syndromes ... KeyWorlds.com , a Piggyback.com company. Updated Friday, 21 September 2001 at 15:43:36 by LinkMaster Search by keywords: Free Inkjet Cartridge?

73. Interactive Fly, Drosophila waardenburg syndrome (WS) types I, II, and III are related autosomal dominantdisorders characterized by sensorineural hearing loss, dystopia canthorum http://sdb.bio.purdue.edu/fly/segment/paird2b.htm

paired EVOLUTIONARY HOMOLOGS Table of contents Mutation of PAX3 The molecular basis of the mouse mutation splotch (Sp) , which is associated with spina bifida and exencephaly, was analyzed at three of its alleles, Sp, Sp2H , and Spr . The paired box gene Pax-3 maps within the Inha to interval, near or at the Sp locus on chromosome 1, and Pax-3 appears to be deleted in heterozygous Spr/+ mice. Analysis of genomic DNA and cDNA clones constructed from embryos identifies a deletion of 32 nucleotides in the Pax-3 mRNA transcript and gene. This deletion maps within the paired homeodomain of PAX-3 and is predicted to create a truncated protein as a result of a newly created termination codon at the deletion breakpoint. This study provides evidence for a causal link between deletion of the paired homeodomain of Pax-3 and the mutation, and infers that Pax-3 plays a key role in normal neural development (Epstein, 1991). The splotch (Sp) mouse mutant displays defects in neural tube closure in the form of exencephaly and spina bifida. A complex mutation in the Pax-3 gene including an A>T transversion at the invariant 3' AG splice acceptor of intron 3 has been identified in the Sp/Sp mutant. This genomic mutation abrogates the normal splicing of intron 3, resulting in the generation of four aberrantly spliced mRNA transcripts. Two of these

74. Health Library - Waardenburg Syndrome Search. World class medicine. Hometown commitment. waardenburg syndrome. Waardenburgsyndrome is a genetic disorder that may be evident at birth (congenital). http://www.phoebeputney.com/library/healthguide/IllnessConditions/topic.asp?hwid

75. Hair, Baldness, Hair Disease, Alopecia, Excess Hair, And Treatments - Reference Click Here. Reference. Chang T, Hashimoto K, Bawle EV. Spontaneous contraction ofleukodermic patches in waardenburg syndrome. J Dermatol 1993 Nov;20(11)70711. http://www.keratin.com/as/as013ref006.shtml

reference Home Forums Privacy Advertising ... Home Reference Chang T, Hashimoto K, Bawle EV. Spontaneous contraction of leukodermic patches in Waardenburg syndrome. J Dermatol 1993 Nov;20(11):707-11 Navigation Hair Biology Diagnosis / Decisions Androgenetic Alopecia Alopecia Areata ... http://www.keratin.com/

76. Mioti: Medical Condition Condition waardenburg syndrome. MEDLINEplus Waardenberg Syndrome. NORD WaardenburgSyndrome. Information from the National Organization for Rare Disorders. http://www.mioti.com/cat/condition/condition.asp?Cat=Waardenburg

77. WAARDENBURG SYNDROME (Search FastHealth.com) WAARDENBURG SYNDROME 18861979), Dutch ophthalmologist. Waardenburg published his descriptionof Waardenburg's syndrome in 1951. The same syndrome had http://www.fasthealth.com/dictionary/w/Waardenburg_syndrome.php

Dictionary FastHealth Email This! n Dutch ophthalmologist. Waardenburg published his description of Waardenburg's syndrome in 1951. The same syndrome had been reported on by J. van der Hoeve in 1916 and D. Klein in 1950. FastNurse Drug Search Hospital Search Find a Physician ... Dead Links

78. Untitled Document Lalwani AK, et al. Point mutation in the MITF gene causing waardenburg syndrometype II in a threegeneration Indian family. Am J Med Genet. http://lmo.ucsf.edu/respaperscontent.html

79. Health Library - Waardenburg Syndrome Your Health, Advanced Search. waardenburg syndrome. waardenburg syndromeis a genetic disorder that may be evident at birth (congenital). http://www.tetonhospital.org/library/healthguide/IllnessConditions/topic.asp?hwi

80. We Can't Find That Page! Provides a definition of waardenburg's syndrome, problems associated with raising a deaf cat and what test is used to diagnose deafness. http://parentzone.com/petzone/health/cat/20034.htm

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