Familial Simpson–Golabi–Behmel syndrome: studies of X‐chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations
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N. Matsumoto | K. Moseley | Y. Watanabe | A. Nishimura | B. Baskin | S. Yano | P. Ray | A. Bagheri | Naomichi Matsumoto | Shoji Yano | Kathryn Moseley | Yoriko Watanabe