Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality

Objective: We present prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome 4 [sSMC(4)] derived from 4q11.1–q12 and q13.2, and 5q13.2 microdeletion with no apparent phenotypic abnormality. Materials and methods: A 32-year-old woma...

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Bibliographic Details
Main Authors: Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Shin-Wen Chen, Peih-Shan Wu, Chien-Wen Yang, Chen-Chi Lee, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang
Format: Article
Language:English
Published: Elsevier 2017-04-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
5q13.2 microdeletion
chromosome 4
mosaicism
prenatal diagnosis
small supernumerary marker chromosome
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455917300189

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http://www.sciencedirect.com/science/article/pii/S1028455917300189

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