Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency-Reference-Cited by-同舟云学术

Prevalence of 22q11 region deletions in patients with velopharyngeal insufficiency

Published:1998-04-28 Issue:1 Volume:77 Page:8-11
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zori Roberto T.,Boyar Fatih Z.,Williams William N.,Gray Brian A.,Bent-Williams Angela,Stalker Heather J.,Rimer Lisa A.,Nackashi John A.,Driscoll Daniel J.,Rasmussen Sonja A.,Dixon-Wood Virginia,Williams Charles A.

Publisher

Wiley

Subject

Genetics (clinical)

Reference29 articles.

1. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

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

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

4. (1995): Are 22q11 chromosomal deletions a major cause of isolated cleft palate? 55th Annual Meeting of the American Cleft Palate-Craniofacial Association. Tampa, FL, April 24-29, 1995 (Abstract 110).

5. Velo-cardio-facial syndrome: A review of 120 patients

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