Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22-Reference-Cited by-同舟云学术

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Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22

Published:2022-03 Issue:2 Volume:61 Page:364-367
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,Chen Ming,Ma Gwo-Chin,Chang Shun-Ping,Chern Schu-Rern,Chen Shin-Wen,Wu Fang-Tzu,Chen Wen-Lin,Lee Meng-Shan,Chen Yun-Yi,Wang Wayseen

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference18 articles.

1. Small supernumerary marker chromosomes (sSMC) in humans;Liehr;Cytogenet Genome Res,2004

2. Handling small supernumerary marker chromosomes in prenatal diagnostics;Liehr;Expert Rev Mol Diagn,2009

3. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics;Liehr;Methods Mol Biol,2008

4. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints;Warburton;Am J Hum Genet,1991

5. Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited;Crolla;Eur J Hum 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. Mosaic Potocki-Lupski Syndrome Due to a Supernumerary Marker Chromosome Containing <i>RAI1</i>;OBM Genetics;2024-03-05

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