The 22q11.2 deletion in African-American patients: An underdiagnosed population?-Reference-Cited by-同舟云学术

The 22q11.2 deletion in African-American patients: An underdiagnosed population?

Published:2005 Issue:3 Volume:134A Page:242-246
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McDonald-McGinn Donna M.,Minugh-Purvis Nancy,Kirschner Richard E.,Jawad Abbas,Tonnesen Melissa K.,Catanzaro Jason R.,Goldmuntz Elizabeth,Driscoll Deborah,LaRossa Don,Emanuel Beverly S.,Zackai Elaine H.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

2. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

3. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

4. 1974. Normal values for selected physical parameters: An aid to syndrome delineation. Birth Defects: Original Article Series 10.

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