Endocrine Manifestations of Chromosome 22q11.2 Microdeletion Syndrome-Reference-Cited by-同舟云学术

Endocrine Manifestations of Chromosome 22q11.2 Microdeletion Syndrome

Published:2005 Issue:6 Volume:63 Page:294-299
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Choi Jin-Ho,Shin Young-Lim,Kim Gu-Hwan,Seo Eul-Ju,Kim Youngho,Park In-Sook,Yoo Han-Wook

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. The 22q11.2 deletion syndrome.

2. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes

3. Shprintzen RJ: Velo-cardio-facial syndrome; in Cassidy SB, Allanson JE (eds): Management of Genetic Syndromes. New York, Wiley-Liss, 2001, pp 495-516.

4. Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletion

5. Phenotype of adults with the 22q11 deletion syndrome: A review

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