61. The 18-23-week Scan - Appendix II Atelosteogenesis Campomelic dysplasia Jarcho–Levin syndrome Achondrogenesis HypophosphatasiaDyssegmental dysplasia cleidocranial dysplasia, Short thorax http://www.fetalmedicine.com/18-23scanbook/Appendix/appII_tbl01.htm

The 18-23-week scan Appendix II Antenatal sonographic findings in skeletal dysplasias Type of limb shortening Rhizomelia Thanatophoric dysplasia Atelosteogenesis Chondrodysplasia punctata (rhizomelic type) Diastrophic dysplasia Congenital short femur Achondroplasia Mesomelia Mesomelic dysplasia COVESDEM association Acromelia Micromelia Achondrogenesis Atelosteogenesis Short-rib polydactyly syndrome (types I and III) Diastrophic dysplasia Fibrochondrogenesis Osteogenesis imperfecta (type II) Kniest dysplasia Dyssegmental dysplasia Altered thoracic dimensions Long narrow thorax Asphyxiating thoracic dysplasia Metatropic dysplasia Fibrochondrogenesis Atelosteogenesis Campomelic dysplasia Achondrogenesis Hypophosphatasia Dyssegmental dysplasia Cleidocranial dysplasia Short thorax Osteogenesis imperfecta (type II) Hypoplastic thorax Short-rib polydactyly syndrome (types I and II) Thanatophoric dysplasia Cerebro-costo-mandibular syndrome Cleidocranial dysostosis syndrome Homozygous achondroplasia Fibrochondrogenesis Otopalatodigital syndrome (type II) Hand and foot abnormalities Postaxial polydactyly Chondroectodermal dysplasia Short rib-polydactyly syndrome (type I, type III)

62. Cleidocranial Dysostosis Cleidocranial dysostosis or cleidocranial dysplasia is syndrome consistingof delayed ossification of midline structures. The syndrome http://www.stevensorenson.com/residents6/cleidocranial_dysostosis.htm

Home Up [ Cleidocranial dysostosis ] Melorheostosis Osteopathia striata Osteopetrosis Osteopoikilosis ... Camurati-Engelmann disease Cleidocranial dysostosis or cleidocranial dysplasia is syndrome consisting of delayed ossification of midline structures. The syndrome is autosomal dominant and affects bones formed intramembraneously. The disease results in short stature. REFERENCES Altschuler EL. Cleidocranial dysostosis and the unity of the Homeric epics: an essay. Clin Orthop. 2001 Feb;(383):286-9. Stewart PA, Wallerstein R, Moran E, Lee MJ. Early prenatal ultrasound diagnosis of cleidocranial dysplasia. Ultrasound Obstet Gynecol. 2000 Feb;15(2):154-6. Click on an image below for additional information: BACK

63. Service Page - Pathologie Information DISEASE Yunis varon syndrome, Synonym(s) cleidocranial dysplasia micrognathiaabsent thumbs, CIM Q87.8, MIM 216340, Sign(s) of the disease (26), http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=3472

64. Medicalseek - Search Engine For The Healthcare Industry Conditions and DiseasesRare Disorderscleidocranial dysplasia Baylor College ofMedicine An article entitled A Natural History of cleidocranial dysplasia. http://www.medicalseek.net/Conditions_and_Diseases_Rare_Disorders_Cleidocranial_

CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Rare Disorders Cleidocranial Dysplasia Conditions and Diseases:Rare Disorders:Cleidocranial Dysplasia Baylor College of Medicine An article entitled: A Natural History of Cleidocranial Dysplasia. faseb.org/genetics/ashg99/f181.htm Cleidocranial Dysplasia Contains information about this rare genetic disorder, chat and more topics for discussion. themrswebdirectory.com/ccdindex Cleidocranial Dysplasia Find information about this rare genetic disorder, chat and more topics for discussion. cleidocranial_dysplasia.homestead.com/page1... MedicineNet.com: Medical Dictionary An explanation of what cleidocranial dysplasia is and how it is transmitted. medicinenet.com/Script/Main/Art.asp?li=... National Library of Medicine: CCD, CLCD A list of synonyms of sleidocranial dysplasia, along with a summary and major features. nlm.nih.gov/mesh/jablonski/syndromes/sy... Readers Digest Health Cleidocranial dysplasia, a list of alternate names, a general discussion and further resources. rd.com/common/nav/index.jhtml?articleId...

65. Cleidocranial Dysostosis Alternative Names cleidocranial dysplasia. Causes, incidence, and risk factorsCleidocranial dysostosis is inherited as an autosomal dominant characteristic. http://www.umm.edu/ency/article/001589.htm

Disease Nutrition Surgery Symptoms Injury ... Z Related Programs at UM Medical Center Department of Orthopaedics Home Medical Reference Encyclopedia (English) Toggle English Spanish Cleidocranial dysostosis Overview Symptoms Treatment Prevention Definition: An autosomal dominant inherited disorder of bony development characterized by absent or incompletely formed collar bones, characteristic facial appearance, short stature, and dental abnormalities. Alternative Names: Cleidocranial dysplasia Causes, incidence, and risk factors: Cleidocranial dysostosis is inherited as an autosomal dominant characteristic. It is equally common in males and females. If one parent is affected, the child has a 50% probability of having the disease. A heavy protruding brow, protruding jaw, wide nasal bridge, and abnormal misaligned teeth characterize the disorder. The incomplete development or absence of the collar bones allows the shoulders to be brought together in front of the body. Other bony abnormalities exist. Intelligence is normal. Review Date: 5/18/2001 Reviewed By: Thomas T, Jeneby, M.D., Division of Plastic Surgery, University of Pennsylvania Medical Center Philadelphia, PA. Review provided by VeriMed Healthcare Network.

66. BCM - Developmental Biology - Brendan Lee Missense mutations abolishing DNA binding domain of the OsteoblastSpecificTranscription Factor CBFA1/OSF2 in cleidocranial dysplasia. http://www.bcm.tmc.edu/db/db_fac-lee.html

Brendan Lee E-mail: blee@bcm.tmc.edu Associate Professor, Baylor College of Medicine Associate Investigator , Howard Hughes Medical Institute B.S., City University of New York, Brooklyn College, 1986 M.D./Ph.D., State University of New York Health Science Center at Brooklyn, 1993 Postdoc, Mount Sinai School of Medicine, NY, 1990-91 Fellow, Baylor College of Medicine, Houston, TX, 1995-98 Genetic pathways that specify development and homeostasis: translational studies of skeletal and kidney development, and therapy for metabolic diseases and In contrast to developmental pathways, much basic information is already available in well studied biochemical pathways that are critical for homeostasis, such as the urea cycle. With this already in hand, we have attempted to translate the basic information into stable isotope based metabolic protocols in urea cycle patients to develop new tools for diagnosis and clinical management. By using this unique human disease model and physiologic tools that measure the in vivo activity of this pathway, we are asking questions about the interaction of the urea cycle and other biochemical pathways that constitute key gene-nutrient interactions during postnatal growth and development. The ultimate goal is to translate information from these well studied pathways into treatment. This is the focus of our gene replacement studies using helper-dependent adenoviral vectors in urea cycle disorders. An integral component of this is work focused on understanding and preventing the host innate immune response and acute toxicity associated with adenovirus treatment. The spectrum of my research program extends from gene identification in human disease, to correlating mechanisms of disease with normal biological processes, to measuring and manipulating these pathways for diagnosis and treatment in humans and in animal models.

67. Cell & Molecular Biology - Applicants/Faculty & Research - Brendan Lee, M.D./Ph. differentiation, we are studying the function of human CBFA1, a runt domain osteoblasttranscriptional factor, in cleidocranial dysplasia and associated http://www.bcm.tmc.edu/cmb/applicants/facres/faculty_res_lee.html

Faculty and their Research Index Brendan Lee, M.D., Ph.D. Associate Professor, Department of Molecular and Human Genetics Director, Skeletal Dysplasia Clinic B.S., City University of New York, Brooklyn College BA/MD Program, N.Y. Ph.D., M.D., State University of New York Health Science Center at Brooklyn, N.Y. RESEARCH INTERESTS: We are interested in isolating and characterizing determinants of cartilage and skeletal development with emphasis on transcriptional regulators of these processes. In the area of bone and cartilage differentiation, we are studying the function of human CBFA1, a runt domain osteoblast transcriptional factor, in cleidocranial dysplasia and associated disorders. As part of these studies, we are generating transgenic mice harboring mutations in an unique polyglutamine/polyalanine domain thought to be important in transcriptional activation and isolating interacting proteins which modify its actions during development. Similarly, CBFA1 has a role during chondrocyte differentiation and parallel studies are aimed at elucidating its transcriptional targets during chondrocyte hypertrophy. In the area of skeletal patterning, we are studying a LIM homeodomain gene, LMX1B, which we have shown to be involved in defective patterning of the skeleton and soft tissues in the condition, nail patella syndrome (NPS). Because of renal involvement in NPS, we are also studying the role of LMX1B during podocyte differentiation.

68. Bjorn R. Olsen, M.D., Ph.D. - The Forsyth Institute cleidocranial dysplasia, a condition characterized by delayed suture ossificationin the skull, supernumerary teeth, and missing clavicles, was found to be http://www.forsyth.org/re/re_i_olsen.htm

Research Focus Areas Departments Investigators ... Health Other investigators Bartlett, John D. Chen, George Dewhirst, Floyd E. Dogon, I. Leon Duncan, Margaret Goodson, J. Max Haffajee, Anne D. Holt, Stanley C. Kawai, Toshihisha Kent, Ralph Levin, Michael Li, Yi-Ping Maiden, Mark F. J. Margolis, Henry C. Niederman, Richard Olsen, Bjorn R. Paster, Bruce J. Skobe, Ziedonis Smith, Daniel J. Socransky, Sigmund S. Soparkar, Pramod M. Stashenko, Philip P. Tanner, Anne Taubman, Martin A. Tavares, Mary Yelick, Pamela C. Bjorn R. Olsen, M.D., Ph.D. Senior Member of the Staff Department of Oral Biology University of Oslo, M.D., 1967, Medicine University of Oslo, Ph.D., 1967, Histology Professor of Cell Biology, Harvard Medical School Professor and Chairman, Harvard-Forsyth Department of Oral Biology STAFF Assistant Member of the Staff I Ernst Reichenberger, Ph.D. Staff Associate Paloma Valverde, Ph.D. Postdoctoral Fellows Eileen Boye, Ph.D.

69. Department Of Biomineralization - The Forsyth Institute scientists have identified the genes that cause several syndromes that affect theface, including cherubism, cleidocranial dysplasia, and craniometaphyseal http://www.forsyth.org/re/re_overview.htm

Research Focus Areas Departments Investigators ... Research Training and Fellowship Opportunities Center for Children's Oral and Craniofacial Health Center for Children's Oral and Craniofacial Health The Face : The face is at the very core of human identity. Self-image and self-esteem are intimately connected with appearance. The faces of children should be radiant-with happiness, excitement, and well being-and embody the ideal of potential for human perfection. The Facts One third of U.S. children suffer from serious oral health problems that leave their faces flawed Discolored, decayed and abscessed teeth are painful and debilitating, and have severe psychological and social consequences. Periodontal diseases cause similar devastation in adults. New research has shown that the causative infections for periodontal disease and dental decay are acquired in early childhood. Periodontal disease in mothers during pregnancy is a risk factor for premature birth, low birth weight, and associated lifelong problems. The oral cavity and craniofacial complex is the site of symptoms of over 120 chronic systemic diseases. Oral infections have also been linked as risk factors for cardiovascular disease, stroke, pulmonary disease, and diabetes

70. Cleidocranial Dysplasia Website Results :: Linkspider UK cleidocranial dysplasia Websites from the Linkspider UK. cleidocranial dysplasiaDirectory. Complete Results for cleidocranial dysplasia Related Topics. http://www.linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/Cleidocra

Cleidocranial Dysplasia Websites from Linkspider UK Keyword: Cleidocranial Dysplasia Linkspider UK Directory Cleidocranial Dysplasia Search for Directory Tree: Top Health Conditions and Diseases Rare Disorders : Cleidocranial Dysplasia (6) Add URL Advertise Here! Personalize Amazon ... Weather See Also: Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Musculoskeletal Disorders National Library of Medicine: CCD, CLCD - A list of synonyms of sleidocranial dysplasia, along with a summary and major features. Cleidocranial Dysplasia - Find information about this rare genetic disorder, chat and more topics for discussion. Baylor College of Medicine - An article entitled: A Natural History of Cleidocranial Dysplasia. MedicineNet.com: Medical Dictionary - An explanation of what cleidocranial dysplasia is and how it is transmitted. Readers Digest Health - Cleidocranial dysplasia, a list of alternate names, a general discussion and further resources. Cleidocranial Dysplasia - Contains information about this rare genetic disorder, chat and more topics for discussion.

71. Yunis Varon Syndrome defective growth of the bones of the skull along with complete or partial absenceof the shoulder blades (cleidocranial dysplasia); characteristic facial http://bchealthguide.org/kbase/nord/nord1094.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord1094"; var hwDocTitle="Yunis Varon Syndrome"; var hwRank="1"; var hwSectionHWID="nord1094"; var hwSectionTitle=""; var hwSource="cn1.6"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Yunis Varon Syndrome Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Cleidocranial Dysplasia Mandibuloacral Dysplasia General Discussion Symptoms Yunis-Varon Syndrome is an extremely rare inherited multisystem disorder characterized by growth retardation prior to and after birth; defective growth of the bones of the skull along with complete or partial absence of the shoulder blades (cleidocranial dysplasia); characteristic facial features; and/or abnormalities of the fingers and/or toes. In most cases, growth delays occur before birth (intrauterine growth retardation) and may result in low birth weight. In most cases, growth delays continue after birth (postnatally). As infants with Yunis-Varon Syndrome mature, they may also exhibit failure to gain weight or grow at the expected rate (failure to thrive), severe developmental delays, and/or mild mental retardation. Failure to thrive results from feeding and respiratory problems. In some cases, feeding and respiratory difficulties may result in life-threatening complications.

72. Multipals My other sites TheMrsWebDirectory.com cleidocranial dysplasia. Picutes of my quadruplets. . . My other sites TheMrsWebDirectory.com cleidocranial dysplasia. http://multipals.homestead.com/

My other sites: TheMrsWebDirectory.com cleidocranial dysplasia Picutes of my quadruplets This page was last updated on: December 15, 2002 This site was created to be a free resource for people who have multiples or are relatives of multiples. Picutes of my quadruplets I have quadruplets and I wanted to find a place to share with others on the internet but I was unable to find one that was free. So I made one My other sites: TheMrsWebDirectory.com cleidocranial dysplasia

73. PCSO Bulletin, Fall 2002 Presentation Summary: "Understanding Impacted Teeth – within dentigerous cysts and teeth that resorb the roots of adjacent teeth (Lecture3) as well as multiple impactions and cleidocranial dysplasia (Lecture 4). http://www.pcsortho.org/bulletin/bulletin02/fa02becker.html

Advanced Search Fall 2002 Presentation Summary: "Understanding Impacted Teeth – Then Treating Them Successfully" Presented by Dr. Adrian Becker, BDS, LDS, RCS, DDO, RCPS, on May 31, 2002, at the Southern Region Meeting. Summarized by Dr. Hong B. Moon, Southern Region Editor Dr. Becker began his lecture series focusing on the etiology, diagnosis and treatment planning of impacted teeth ( Lecture 1 Then he specifically presented the rationale for treating unerupted, dilacerated and severely traumatized incisor teeth and ways of dealing with severely displaced maxillary canines and other teeth ( Lecture 2 This lecture also covered teeth from within dentigerous cysts and teeth that resorb the roots of adjacent teeth ( Lecture 3 ) as well as multiple impactions and cleidocranial dysplasia ( Lecture 4 Dr. Becker stressed the treatment of impacted teeth in the context of an overall orthodontic treatment strategy. Lecture 1: Radiology The aims of radiology in relation to impacted teeth are (1) to find the pathology such as supernumerary teeth, cystic damage, ankylosis, abnormality of crown or root, resorption of crown or root, and (2) to find the location using tube-shift method (lateral or vertical shift), panoramic view, views at right angles, and/or computed tomography. The position of the apex of the tooth determines its prognosis, and this is not possible to mentally reconstruct from a pair of periapical films alone.

74. JPS 105-04e 2. Clinical and Genetic Analysis of cleidocranial dysplasia in Japan. Title.Clinical and Genetic Analysis of cleidocranial dysplasia in Japan. Author. http://www.jpeds.or.jp/english/journal/105-04e.html

75. Cleidocranial Dysplasia cleidocranial dysplasia. A Medical Medical System. A resource with informationon over 4000 medical topics including cleidocranial dysplasia. http://www.bloodandmarrowtransplant.com/medical-terms/04035.htm

Cleidocranial dysplasia A Medical Encyclopedia Article provided by Maryland General Hospital A resource with information on over 4000 medical topics including: Cleidocranial dysplasia Previous Next

76. PAEDIATRIC BONE DISORDERS known as Trevors Disease Progressive Diaphyseal Dysplasia AD MucopolysaccharidosisDiastrophic Dysplasia - AR cleidocranial dysplasia - AD Benign Bone http://www.worldortho.com/database/etext/bone_disorders.html

PAEDIATRIC BONE DISORDERS Background info: Dwarfism can be PROPORTIONATE - manifesting a symmetric decrease in both truncal and limb length. Dwarfism can be DISPROPORTIONATE - manifesting either a short limb disorder or a short trunk disorder. Short - limbed dwarfism can affect either the proximal, the middle or the distal region of a limb. FORMS OF DYSPLASIA include: Achondroplasia Spondyloepiphyseal Dysplasia Chondrodysplasia Punctalta Kneist Syndrome - AD Metaphyseal chondrodysplasia Multiple Epiphyseal Dysplasia Dysplasia Epiphysiallis Haemimeliea [known as Trevors Disease] Progressive Diaphyseal Dysplasia - AD Mucopolysaccharidosis Diastrophic Dysplasia - AR Cleidocranial Dysplasia - AD Benign Bone Growth Dysplasia A) Achondroplasia Achondroplasia is the most common form of disproportionate dwarfism. It is an autosomal dominant (AD) condition with an 80% spontaneous mutation. It is caused by abnormal endochondral bone formation [in the proliferative zone] and can be associated with late-in-life childbirth. It is a quantitative [not a qualitative] cartilage defect. The afflicted child will have dwarfed limbs and a normal trunk.

77. Cleidocranial Dysplasia The summary for this Ukrainian page contains characters that cannot be correctly displayed in this language/character set. http://ibis-birthdefects.org/start/ukrainian/ucleidys.htm

Please set browser to encoding in cyrillic...) Ïðî I.B.I.S. Ïðèºäíàéòåñü äî I.B.I.S. Ïîðóøåííÿ ïðîöåñ³â îñèô³êàö³¿ ïðîÿâëÿºòüñÿ ³íîä³ â ìíîæèííèõ spina bifida â³ä øèéíèõ äî ïîïåðåêîâèõ â³ää³ë³â õðåáòà, â äîäàòêîâèõ ÿäðàõ îêîñòåí³ííÿ ïîïåðå÷íèõ â³äðîñòê³â. Ðåíòãåíîëîã³÷íà êàðòèíà ÷åðåïíî - êëþ÷è÷íî¿ äèñïëà糿 äóæå õàðàêòåðíà. ×èì ìåíøà äèòèíà, òèì çì³íè â ñòðóêòóð³ ÷åðåïà ïîì³òí³ø³: áðàõ³öåôàë³ÿ, ê³ñòêè òîíê³, øâè ðîçøèðåí³, â íèõ äîäàòêîâ³ ê³ñòêîâ³ âêðàïëåííÿ - âîð쳺Ⳡê³ñòî÷êè. Ïðîâ³äíèé Rg-ñèìïòîì - çì³íè â êëþ÷èöÿõ. Ïðåíàòàëüíà ÓÇÄ ìîæëèâà, àäæå êëþ÷èö³ ïëîäà ëåãêî ïîì³òí³, àëå ã³ïîïëàç³ÿ ³ â³äñóòí³ñòü êëþ÷èöü íå ïàòîãíîìîí³÷íà äëÿ ÷åðåïíî - êëþ÷è÷íî¿ äèñïëà糿, îñê³ëüêè çóñòð³÷àºòüñÿ ³ ïðè ³íøèõ çàõâîðþâàííÿõ. Cleidocranial Dysplasia, Recessive Form Jones KL. Smith's Recognizable Patterns of Human Malformation. Philadelphia: W.B. Saunders Company, 1997:408. Warkany J. Congenital Malformations: Notes and Comments. Chicago: Year Book Publisher, 1981:836-840. Êîçëîâà Ñ.È., Äåìèêîâà Í.Ñ., Ñåìàíîâà Å., Áëèííèêîâà Î.Å. Íàñëåäñòâåííûå ñèíäðîìû è ìåäèêî - ãåíåòè÷åñêîå êîíñóëüòèðîâàíèå.- Ì.: Ïðàêòèêà,1996.- C. 312-313. Øóêàòè â IBIS FreeFind ²íôîðìàö³ÿ íà ö³é ñòîð³íö³ º âèêëþ÷íî òî÷êîþ çîðó ¿¿ àâòîðà, ÿêó íå îáîâ’ÿçêîâî ïîä³ëÿþòü Óêðà¿íñüêî-Àìåðèêàíñüêà Ïðîãðàìà çàïîá³ãàííÿ âðîäæåíèì âàäàì ðîçâèòêó, Àìåðèêàíñüêà Ôóíäàö³ÿ “March of Dimes” ÷è áóäü-ÿêà ³íøà ïîä³áíà îðãàí³çàö³ÿ. Íàø ñàéò ïðîïîíóº ³íôîðìàö³þ ïåðåâàæíî ç ìåòîþ ðîçïîâñþäæåííÿ ìåäè÷íèõ çíàíü. Íå âèêîðèñòîâóéòå éîãî â ÿêîñò³ ºäèíîãî äæåðåëà ìåäè÷íî¿ ³íôîðìàö³¿, àáî ùîá ñàìîñò³éíî çì³íèòè ïðîöåñ ë³êóâàííÿ. Áóäü ëàñêà, ïðî÷èòàéòå ïîâíèé òåêñò

78. ´ëÇѱ¸°­¾Ç¾È¸é¹æ»ç¼±ÇÐȸ cleidocranial dysplasia Report of a Case. Jeong SJ, Hong SK. Department of Oraland Maxillofacial Radiology, College of Dentistry, Chosun University, Korea. http://www.kaomfr.org/2000/abstract/229a.html

Korean J Oral Maxillofac Radiol . 2000 Sep;30(3):229-234. Korean. Cleidocranial Dysplasia: Report of a Case. Jeong SJ, Hong SK. Department of Oral and Maxillofacial Radiology, College of Dentistry, Chosun University, Korea. djsj6042@hanmail.net

79. Abstracts that underlie skeletal pathology, the molecular basis of a patterning defect, synpolydactyly,and a defect of organogenesis, cleidocranial dysplasia, will be http://www.novartisfound.org.uk/catalog/232abs.htm

Abstracts Genetic control of skeletal development Gerard Karsenty Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA There are three major topics of skeleton biology. The first is skeleton patterning which addresses how the shape and the location of each specific skeletal element is achieved. The second topic is cell differentiation in the skeleton. There are three specific cell types in the skeleton: the chondrocyte in cartilage, the osteoblast and the osteoclast in bone. The first two cell types are from mesenchymal origin while the third is from monocytic origin. The genes controlling skeleton patterning and cell differentiation are for the most part different. The third aspect of skeleton biology addresses the molecular control of the major function of the skeleton such as skeleton growth, bone mineralization and bone remodelling. Our current knowledge in each of these areas of skeleton biology will be presented in broad terms to set the course for other presentations during the symposium. Return to contents ©2001 The Novartis Foundation Early steps in limb patterning and chondrogenesis Sandrine Pizette and Lee Niswander Molecular Biology Program and Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA

80. [Frontiers In Bioscience 3, D834-837, August 1, 1998] KC Gilmour, IR Rosewell, GWH Stamp, RSP Beddington, S. Mundlos, BR Olsen, PB Selby MJ Owen Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is http://www.bioscience.org/1998/v3/d/karsenty/8.htm

[Frontiers in Bioscience 3, d834-837, August 1, 1998] Reprints PubMed CAVEAT LECTOR TRANSCRIPTIONAL REGULATION OF OSTEOBLAST DIFFERENTIATION DURING DEVELOPMENT Gerard Karsenty Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030 Received 2/18/98 Accepted 3/23/98 8. REFERENCES 1. Hogan B.L.M.: Bone morphogenetic proteins: multifunctional regulators of vertebrate development. Curr. Opin. Genet. Dev. 3. Orkins S.H: Transcription factors and hematopoietic development. J. Biol. Chem. Nature Proc. Natl. Acad. Sci. USA Cell Mol. Cell. Biol. 8. Geoffroy, V., J. Biol. Chem. Runt domain transcription factor family: interactions with the osteocalcin gene promoter. Biochemistry runt Dev. Biol. Trends in Genetics Mol. Cell. Biol. Cell , a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell 16. Komori, T., H. Yagi, S. Nomura, A. Yamaguchi, K. Sasaki, K. Deguchi, Y. Shimizu, R.T. Bronson, Y-H. Gao, M. Inada, M. Sato, R. Okamoto, Y. Kitamura, S. Yoshiki, T. Kishimoto: Targeted disruption of results in a complete lack of bone formation owing to maturational arrest of osteoblasts.

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