Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice-Reference-Cited by-同舟云学术

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice

Published:2009-10-12 Issue: Volume: Page:
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Randall Victoria,McCue Karen,Roberts Catherine,Kyriakopoulou Vanessa,Beddow Sarah,Barrett Angela N.,Vitelli Francesca,Prescott Katrina,Shaw-Smith Charles,Devriendt Koen,Bosman Erika,Steffes Georg,Steel Karen P.,Simrick Subreena,Basson M. Albert,Illingworth Elizabeth,Scambler Peter J.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference63 articles.

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2. Role of TBX1 in human del22q11.2 syndrome

3. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome

4. Human TBX1 Missense Mutations Cause Gain of Function Resulting in the Same Phenotype as 22q11.2 Deletions

5. Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

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