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