Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin-Reference-Cited by-同舟云学术

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Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin

Published:2020-09 Issue:5 Volume:59 Page:766-769
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,Wang Liang-Kai,Chern Schu-Rern,Wu Peih-Shan,Chen Shin-Wen,Wu Fang-Tzu,Chen Yun-Yi,Chen Wen-Lin,Chen Li-Feng,Wang Wayseen

Funder

Ministry of Science and Technology, Taiwan

MacKay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference10 articles.

1. 14q32 deletion syndrome: a clinical report;Youngs;Clin Dysmorphol,2012

2. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints;Chen;Gene,2013

3. Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype;Hosoki;Eur J Hum Genet,2008

4. Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes;Kagami;Nat Genet,2008

5. The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers;Kagami;PLoS Genet,2010

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Many faces and functions of GSKIP: a temporospatial regulation view;Cellular Signalling;2022-09

2. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26

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