Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly-Reference-Cited by-同舟云学术

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly

Published:1988-09 Issue:1 Volume:31 Page:1-4
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Greenberg Frank,Courtney Kristine B.,Wessels Robert A.,Huhta James,Carpenter Robert J.,Rich Donna C.,Ledbetter David H.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics(clinical)

Reference11 articles.

1. The spectrum of the DiGeorge syndrome

2. Syndromes with lissencephaly. I: Millerdieker and Norman-Roberts syndromes and isolated lissencephaly

3. Miller-Dieker syndrome: Lissencephaly andmonosomy 17p

4. Familial DiGeorge syndrome and associated partial monosomy of chromosome 22

5. Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17

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