Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review-Reference-Cited by-同舟云学术

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review

Published:2020-11 Issue:6 Volume:59 Page:963-967
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Sun Mei-Ling,Zhang Hong-Guo,Liu Xiang-Yin,Yue Fa-Gui,Jiang Yu-Ting,Li Shi-Bo,Liu Rui-Zhi

Funder

Finance Department Health Special Project of Jilin Province

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference22 articles.

1. The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype;Santacroce;Syst Biol Reprod Med,2015

2. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review;Chen;Taiwan J Obstet Gynecol,2017

3. Molecular cytogenetic diagnostics of marker chromosomes: analysis in four prenatal cases and long-term clinical evaluation of carriers;Tesner;Cytogenet Genome Res,2018

4. Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations;Haddad;Am J Med Genet,2012

5. Complex small supernumerary marker chromosome leading to partial 4q21q duplications clinical implication and review of the literature;Bellucco;Cytogenet Genome Res,2018

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