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

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.

Source: Taiwanese Journal of Obstetrics and Gynecology - April 1, 2017 Category: OBGYN 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 Tags: Short Communication Source Type: research