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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).
Yoshimura-Furuhata M, Nishimura-Tadaki A, Amano Y, Ehara T, Hamasaki Y, Muramatsu M, Shishido S, Aikawa A, Hamada R, Ishikura K, Hataya H, Hidaka Y, Noda S, Koike K, Wakui K, Fukushima Y, Matsumoto N, Awazu M, Miyake N, Kosho T. Yoshimura-Furuhata M, et al. Among authors: hamada r. Am J Med Genet A. 2015 Mar;167A(3):592-601. doi: 10.1002/ajmg.a.36942. Am J Med Genet A. 2015. PMID: 25691411 Review.
282 results