Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma-Reference-Cited by-同舟云学术

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Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma

Published:2015-02 Issue:1 Volume:54 Page:78-80
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,Ko Tsang-Ming,Huang Ming-Chao,Chern Schu-Rern,Lin Tan-Wei,Chang Tung-Yao,Kuo Yu-Ling,Chen Wen-Lin,Wang Wayseen

Funder

Ministry of Science and Technology

Mackay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference13 articles.

1. Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly, and cebocephaly in a fetus;Chen;Prenat Diagn,1998

2. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 by amniocentesis;Chen;Taiwan J Obstet Gynecol,2009

3. Trisomy 13 ascertained in a survey of spontaneous abortions;Jacobs;J Med Genet,1987

4. Unbalanced Robertsonian translocations associated with Down's syndrome or Patau's syndrome: chromosome subtype, proportion inherited, mutation rates, and sex ratio;Hook;Hum Genet,1981

5. Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases;Bugge;Am J Med Genet,2005

Cited by 1 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. Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case;Annales de biologie clinique;2017-11

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