Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family

Objective: This study was aimed at detection of recurrent transmission of the 17q12 microdeletion in a fetus with congenital anomalies of the kidney and urinary tract. Materials and Methods: A 35-year-old woman was referred to the hospital at 20 weeks' gestation because of hydronephrosis in the...

Full description

Bibliographic Details

Published in:	Taiwanese Journal of Obstetrics & Gynecology
Main Authors:	Chih-Ping Chen, Shuenn-Dyh Chang, Tzu-Hao Wang, Liang-Kai Wang, Jeng-Daw Tsai, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang
Format:	Article
Language:	English
Published:	Elsevier 2013-12-01
Subjects:	17q12 microdeletion HNF1B hydronephrosis LHX1 multicystic kidney
Online Access:	http://www.sciencedirect.com/science/article/pii/S1028455913001800