Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice-Reference-Cited by-同舟云学术

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

Published:2001-03 Issue:6824 Volume:410 Page:97-101
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Lindsay Elizabeth A.,Vitelli Francesca,Su Hong,Morishima Masae,Huynh Tuong,Pramparo Tiziano,Jurecic Vesna,Ogunrinu George,Sutherland Helen F.,Scambler Peter J.,Bradley Allan,Baldini Antonio

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/35065105.pdf

Reference26 articles.

1. Scambler, P. J. The 22q11 deletion syndromes. Hum. Mol. Genet. 9, 2421–2426 (2000).

2. Lindsay, E. A. et al. Congenital heart disease in mice deficient for the DiGeorge syndrome region. Nature 401, 379–383 (1999).

3. O'Donnell, H., McKeown, C., Gould, C., Morrow, B. & Scambler, P. Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region. Am. J. Hum. Genet. 60, 1544–1548 (1997).

4. Amati, F. et al. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome. Eur. J. Hum. Genet. 7, 903–909 (1999).

5. McQuade, L. et al. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR). Am. J. Med. Genet. 86, 27–33 (1999).

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