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Results: 4

Authors: Kato, M Kanai, M Soma, O Takusa, Y Kimura, T Numakura, C Matsuki, T Nakamura, S Hayasaka, L
Citation: M. Kato et al., Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis, ANN NEUROL, 50(4), 2001, pp. 547-551

Authors: Miyoshi, O Yabe, R Wakui, K Fukushima, Y Koizumi, S Uchikawa, M Kajii, T Numakura, C Takahashi, S Hayasaka, K Niikawa, N
Citation: O. Miyoshi et al., Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1, AM J MED G, 104(3), 2001, pp. 250-256

Authors: Numakura, C Lin, CQ Oka, N Akiguchi, I Hayasaka, K
Citation: C. Numakura et al., Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1, ANN NEUROL, 47(1), 2000, pp. 101-103

Authors: Lin, CQ Numakura, C Ikegami, T Shizuka, M Shoji, M Nicholson, G Hayasaka, K
Citation: Cq. Lin et al., Deletion and nonsense mutations of the connexin 32 gene associated with Charcot-Marie-Tooth disease, TOH J EX ME, 188(3), 1999, pp. 239-244
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