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, Tomoki Kosho, Masaki Muramatsu et al.|American Journal of Medical Genetics Part A|2015Cited by 15