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

• Main Authors: Chih-Ping Chen (Author), Shuenn-Dyh Chang (Author), Tzu-Hao Wang (Author), Liang-Kai Wang (Author), Jeng-Daw Tsai (Author), Yu-Peng Liu (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Jun-Wei Su (Author), Yu-Ting Chen (Author), Wayseen Wang (Author)
• Format: Book
• Published: Elsevier, 2013-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...