Deciphering the Basis for Congenital Heart Defects Using a Mouse Model of Holt-oram Syndrome-Reference-Cited by-同舟云学术

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Deciphering the Basis for Congenital Heart Defects Using a Mouse Model of Holt-oram Syndrome

Published:2007-11-12 Issue: Volume: Page:121-124
ISSN:
Container-title:Cardiovascular Development and Congenital Malformations
language:
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Author:

Bruneau Benoit G.

Publisher

Blackwell Publishing Ltd

Reference14 articles.

1. Tbx5 is essential for forelimb bud initiation following patterning of the limb field in the mouse embryo;Agarwal;Development,2003

2. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome;Basson;Nat Genet,1997

3. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome);Basson;N Engl J Med,1994

4. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways;Benson;J Clin Invest,1999

5. A targeted disruption in connexin40 leads to distinct atrioventricular conduction defects;Bevilacqua;J Interv Card Electrophysiol,2000

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