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Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features.
Yamada K, Yamada Y, Nomura N, Miura K, Wakako R, Hayakawa C, Matsumoto A, Kumagai T, Yoshimura I, Miyazaki S, Kato K, Sonta S, Ono H, Yamanaka T, Nagaya M, Wakamatsu N. Yamada K, et al. Among authors: yoshimura i. Am J Hum Genet. 2001 Dec;69(6):1178-85. doi: 10.1086/324343. Epub 2001 Oct 2. Am J Hum Genet. 2001. PMID: 11592033 Free PMC article.
Is hiragana decoding impaired in children with periventricular leukomalacia?
Kurahashi N, Futamura Y, Nonobe N, Ogaya S, Maki Y, Yoshimura I, Suzuki T, Hosokawa Y, Yamada K, Aso K, Maruyama K, Nakamura M. Kurahashi N, et al. Among authors: yoshimura i. Brain Dev. 2018 Nov;40(10):850-856. doi: 10.1016/j.braindev.2018.05.018. Epub 2018 Jun 19. Brain Dev. 2018. PMID: 29908673
Clinical evaluation of repeat apheresis donors in Japan.
Furuta M, Shimizu T, Mizuno S, Kamiya T, Ozawa K, Nakase T, Tadokoro K, Takenaka M, Ohkawa T, Yokoyama S, Ogawa Y, Kiyokawa H, Shimizu M, Sekine N, Yoshimura I. Furuta M, et al. Among authors: yoshimura i. Vox Sang. 1999;77(1):17-23. doi: 10.1159/000031069. Vox Sang. 1999. PMID: 10474086
184 results