Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results-Reference-Cited by-同舟云学术

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Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results

Published:2020-09 Issue:5 Volume:59 Page:758-762
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,Liou Jui-Der,Seow Kok-Min,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Wu Fang-Tzu,Town Dai-Dyi,Chen Li-Feng,Wang Wayseen

Funder

Ministry of Science and Technology, Taiwan

MacKay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference37 articles.

1. Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals;Phelan;Am J Med Genet,1995

2. Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37;Wilson;Am J Hum Genet,1995

3. Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes;Aldred;J Med Genet,2004

4. Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype;Shrimpton;Clin Genet,2004

5. Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems;Williams;Am J Hum Genet,2010

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