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

Author:

Chen Chih-Ping,Chang Shuenn-Dyh,Wang Tzu-Hao,Wang Liang-Kai,Tsai Jeng-Daw,Liu Yu-Peng,Chern Schu-Rern,Wu Peih-Shan,Su Jun-Wei,Chen Yu-Ting,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference50 articles.

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3. A molecular and genetic view of human renal and urinary tract malformations;Woolf;Kidney Int,2000

4. HNF1B alterations associated with congenital anomalies of the kidney and urinary tract;Nakayama;Pediatr Nephrol,2010

5. Copy-number disorders are a common cause of congenital kidney malformations;Sanna-Cherchi;Am J Hum Genet,2012

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