Klippel–Feil syndrome associated with situs inversus: Description of a new case and exclusion of GDF1, GDF3 and GDF6 as causal genes-Reference-Cited by-同舟云学术

Klippel–Feil syndrome associated with situs inversus: Description of a new case and exclusion of GDF1, GDF3 and GDF6 as causal genes

Published:2012-06 Issue:6-7 Volume:55 Page:414-417
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Chacón-Camacho Oscar,Camarillo-Blancarte Leyla,Pelaez-González Hugo,Mendiola Jaime,Zenteno Juan C.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference33 articles.

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3. Synergistic interaction between GDF1 and Nodal during anterior axis development;Andersson;Dev. Biol.,2006

4. GDF, a novel locus a spectrum of ocular development anomalies;Asai-Coakwell;Am. J. Hum. Genet.,2007

5. Molecular genetics of heterotaxy syndromes;Belmont;Curr. Opin. Cardiol.,2004

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