Prenatal diagnosis of Smith–Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects-Reference-Cited by-同舟云学术

Prenatal diagnosis of Smith–Magenis syndrome in two fetuses with increased nuchal translucency, mild lateral ventriculomegaly, and congenital heart defects

Published:2016-12 Issue:6 Volume:55 Page:886-890
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Lei Ting-Ying,Li Ru,Fu Fang,Wan Jun-Hui,Zhang Yong-Ling,Jing Xiang-Yi,Liao Can

Funder

Key Program of Guangzhou Health Bureau

Guangzhou Technology and Information of Science

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference28 articles.

1. Multi-disciplinary clinical study of Smith–Magenis syndrome (deletion 17p11.2);Greenberg;Am J Med Genet,1996

2. Gender, genotype, and phenotype differences in Smith–Magenis syndrome: a meta-analysis of 105 cases;Edelman;Clin Genet,2007

3. Interstitial deletion of (17)(p11.2p11.2) in nine patients;Smith;Am J Med Genet,1986

4. Mutations in RAI1 associated with Smith–Magenis syndrome;Slager;Nat Genet,2003

5. Prenatal diagnosis of interstitial deletion of 17p(11.2P11.2) (Smith–Magenis syndrome);Fan;Am J Med Genet,1994

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