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Renal Complications in 6p Duplication Syndrome: Microarray-Based Investigation of the Candidate Gene(s) for the Development of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) and Focal Segmental Glomerular Sclerosis (FSGS).

Megumi Yoshimura-Furuhata,Akira Nishimura-Tadaki,Yoshiro Amano,Takashi Ehara,Yuko Hamasaki,Masaki Muramatsu,Seiichiro Shishido,Atsushi Aikawa,Riku Hamada,Kenji Ishikura,Hiroshi Hataya,Yoshihiko Hidaka,Shunsuke Noda,Kenichi Koike,Keiko Wakui,Yoshimitsu Fukushima,Naomichi Matsumoto,Midori Awazu,Noriko Miyake,Tomoki Kosho

American journal of medical genetics Part A（2015）

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