Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18-Reference-Cited by-同舟云学术

Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18

Published:2010-03 Issue:1 Volume:49 Page:129-132
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Su Yi-Ning,Hsu Chin-Yuan,Ling Pei-Ying,Tsai Fuu-Jen,Chern Schu-Rern,Wu Pei-Chen,Chen Hsiao-En Cindy,Wang Wayseen

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference18 articles.

1. De l'acrocephalosyndactylie;Apert;Bull Mem Soc Med Hop Paris,1906

2. Apert's syndrome (a type of acrocephalosyndactyly): observations on a British series of thirty-nine cases;Blank;Ann Hum Genet,1960

3. Birth prevalence study of the Apert syndrome;Cohen;Am J Med Genet,1992

4. A study of parental age effects on the occurrence of fresh mutations for the Apert syndrome;Erickson;Ann Hum Genet,1974

5. Exclusive paternal origin of new mutations in Apert syndrome;Moloney;Nat Genet,1996

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