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)
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Y. Fukushima | N. Matsumoto | K. Koike | N. Miyake | K. Wakui | T. Ehara | T. Kosho | Y. Amano | K. Ishikura | M. Awazu | R. Hamada | Y. Hamasaki | H. Hataya | S. Shishido | A. Aikawa | A. Nishimura-Tadaki | M. Muramatsu | Megumi Yoshimura-Furuhata | Y. Hidaka | Shunsuke Noda | Akira Nishimura‐Tadaki