Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)-Reference-Cited by-同舟云学术

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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Published:2016-04 Issue:2 Volume:55 Page:288-292
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,Hung Fung-Yu,Chern Schu-Rern,Wu Peih-Shan,Chen Yen-Ni,Chen Shin-Wen,Lee Chen-Chi,Wang Wayseen

Funder

Ministry of Science and Technology (Taipei, Taiwan)

Mackay Memorial Hospital (Taipei, Taiwan)

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference19 articles.

1. Bilateral anterior segment dysgenesis in an infant with partial trisomy 16q and partial monosomy 3p;Dikmetas;J AAPOS,2012

2. Pure partial monosomy 3p (3p25.3→pter): prenatal diagnosis and array comparative genomic hybridization characterization;Chen;Taiwan J Obstet Gynecol,2012

3. Prenatal diagnosis of distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization;Chen;Taiwan J Obstet Gynecol,2013

4. A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family;Moghadasi;Am J Med Genet,2014

5. Del(3)(p25.3) without phenotypic effect;Knight;J Med Genet,1995

Cited by 4 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. Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations;Taiwanese Journal of Obstetrics and Gynecology;2024-07

2. A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature;American Journal of Medical Genetics Part A;2021-06

3. Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation;Medicine;2021-02-19

4. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA , CELF4 and SETBP1;Taiwanese Journal of Obstetrics and Gynecology;2017-12

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