20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder-Reference-Cited by-同舟云学术

20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder

Published:2010-12-28 Issue:1 Volume:155 Page:186-191
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Williams P.G.,Wetherbee J.J.,Rosenfeld J.A.,Hersh J.H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33763/fullpdf

Reference42 articles.

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3. Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2;Ballif;Clin Genet,2008b

4. Holoprosencephaly survival and performance;Barr;Am J Med Genet,1999

5. del(20p) with manifestations of arteriohepatic dysplasia;Byrne;Am J Med Genet,1986

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