TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome-Reference-Cited by-同舟云学术

TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome

Published:2008-11 Issue:5 Volume:83 Page:649-655
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lausch Ekkehart,Hermanns Pia,Farin Henner F.,Alanay Yasemin,Unger Sheila,Nikkel Sarah,Steinwender Christoph,Scherer Gerd,Spranger Jürgen,Zabel Bernhard,Kispert Andreas,Superti-Furga Andrea

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference21 articles.

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2. Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: Three additional cases;Elliott;Am. J. Med. Genet.,2000

3. Dorsoventral patterning of the mouse coat by Tbx15;Candille;PLoS Biol.,2004

4. Genetics of shoulder girdle formation: Roles of Tbx15 and aristaless-like genes;Kuijper;Development,2005

5. The T-box transcription factor Tbx15 is required for skeletal development;Singh;Mech. Dev.,2005

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