Prenatal Diagnosis of Chromosome 22q11.2 Deletions: Experiences in a Single Institution-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of Chromosome 22q11.2 Deletions: Experiences in a Single Institution

Published:2013-12-31 Issue:2 Volume:10 Page:99-103
ISSN:1226-1769
Container-title:Journal of Genetic Medicine
language:en
Short-container-title:J Genet Med

Author:

Chae Yong Hwa¹,Kwak Dong Wook¹,Kim Moon Young¹,Park So Yeon²,Lee Bom Yi²,Lee Yeon Woo²,Lee Young Ho³,Song Mi Jin³,Ryu Hyun Mee¹²

Affiliation:

1. Department of Obstetrics and Gynecology, Cheil General Hospital and Women’s Healthcare Center, Kwandong University College of Medicine, Seoul, Korea

2. Laboratory of Medical Genetics, Cheil Medical Research Institute, Cheil General Hospital and Women’s Healthcare Center, Seoul, Korea

3. Department of Radiology, Cheil General Hospital and Women’s Healthcare Center, Kwandong University College of Medicine, Seoul, Korea

Publisher

Korean Society of Medical Genetics

Subject

General Medicine

Link

http://pdf.medrang.co.kr/JGM/2013/010/KSMGG6_2013_v10n2_99.pdf

Reference20 articles.

1. Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

2. DiGeorge syndrome: part of CATCH 22.

3. The 22q11.2 deletion syndrome.

4. Variable phenotypes in velocardiofacial syndrome with chromosomal deletion

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