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Results: 1-25/29
Authors:
Muroya, K
Sasagawa, I
Suzuki, Y
Nakada, T
Ishii, T
Ogata, T
Citation: K. Muroya et al., Hypospadias and the androgen receptor gene: mutation screening and CAG repeat length analysis, MOL HUM REP, 7(5), 2001, pp. 409-413
Authors:
Tanaka, Y
Sugita, K
Saito, T
Muroya, K
Ishikawa, S
Awazu, M
Ogata, T
Citation: Y. Tanaka et al., Impaired urinary water excretion in a three-generation family, PED NEPHROL, 16(10), 2001, pp. 820-822
Authors:
Ogata, T
Muroya, K
Ohashi, H
Mochizuki, H
Hasegawa, T
Kaji, M
Citation: T. Ogata et al., Female gonadal development in XX patients with distal 9p monosomy, EUR J ENDOC, 145(5), 2001, pp. 613-617
Authors:
Ogata, T
Muroya, K
Ishii, T
Suzuki, Y
Nakada, T
Sasagawa, I
Citation: T. Ogata et al., Undermasculinized genitalia in a boy with an abnormally expanded CAG repeat length in the androgen receptor gene, CLIN ENDOCR, 54(6), 2001, pp. 835-838
Authors:
Suzuki, Y
Sasagawa, I
Tateno, T
Ashida, J
Nakada, T
Muroya, K
Ogata, T
Citation: Y. Suzuki et al., Mutation screening and CAG repeat length analysis of the androgen receptorgene in Klinefelter's syndrome patients with and without spermatogenesis, HUM REPR, 16(8), 2001, pp. 1653-1656
Authors:
Sasagawa, I
Suzuki, Y
Ashida, J
Nakada, T
Muroya, K
Ogata, T
Citation: I. Sasagawa et al., Expansion of the CAG trinucleotide repeats in the androgen receptor gene and male infertility: A controversial association - Response, J ANDROLOGY, 22(5), 2001, pp. 749-749
Authors:
Sasagawa, I
Suzuki, Y
Ashida, J
Nakada, T
Muroya, K
Ogata, T
Citation: I. Sasagawa et al., CAG repeat length analysis and mutation screening of the androgen receptorgene in Japanese men with idiopathic azoospermia, J ANDROLOGY, 22(5), 2001, pp. 804-808
Authors:
Ogata, T
Matsuo, M
Muroya, K
Koyama, Y
Fukutani, K
Citation: T. Ogata et al., 47,XXX male: A clinical and molecular study, AM J MED G, 98(4), 2001, pp. 353-356
Authors:
Muroya, K
Hasegawa, T
Ito, Y
Nagai, T
Isotani, H
Iwata, Y
Yamamoto, K
Fujimoto, S
Seishu, S
Fukushima, Y
Hasegawa, Y
Ogata, T
Citation: K. Muroya et al., GATA3 abnormalities and the phenotypic spectrum of HDR syndrome, J MED GENET, 38(6), 2001, pp. 374-380
Authors:
Ishii, T
Sato, S
Kosaki, K
Sasaki, G
Muroya, K
Ogata, T
Matsuo, N
Citation: T. Ishii et al., Micropenis and the AR gene: Mutation and CAG repeat-length analysis, J CLIN END, 86(11), 2001, pp. 5372-5378
Authors:
Ogata, T
Muroya, K
Matsuo, N
Shinohara, O
Yorifuji, T
Nishi, Y
Hasegawa, Y
Horikawa, R
Tachibana, K
Citation: T. Ogata et al., Turner syndrome and Xp deletions: Clinical and molecular studies in 47 patients, J CLIN END, 86(11), 2001, pp. 5498-5508
Authors:
Suzuki, Y
Sasagawa, I
Ashida, J
Nakada, T
Muroya, K
Ogata, T
Citation: Y. Suzuki et al., Screening for mutations of the androgen receptor gene in patients with isolated cryptorchidism, FERT STERIL, 76(4), 2001, pp. 834-836
Authors:
Sasagawa, I
Suzuki, Y
Tateno, T
Nakada, T
Muroya, K
Ogata, T
Citation: I. Sasagawa et al., CAG repeat length of the androgen receptor gene in Japanese males with cryptorchidism, MOL HUM REP, 6(11), 2000, pp. 973-975
Authors:
Matsuo, M
Muroya, K
Adachi, M
Tachibana, K
Asakura, Y
Nakagomi, Y
Hanaki, K
Yokoya, S
Yoshizawa, A
Igarashi, Y
Hanew, K
Matsuo, N
Ogata, T
Citation: M. Matsuo et al., Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development, HUM GENET, 107(5), 2000, pp. 433-439
Authors:
Adachi, M
Tachibana, K
Asakura, Y
Muroya, K
Ogata, T
Citation: M. Adachi et al., Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features, HUM GENET, 106(3), 2000, pp. 306-310
Authors:
Ogata, T
Wakui, K
Kosho, T
Muroya, K
Yamanouchi, Y
Takano, T
Fukushima, Y
Rappold, G
Suzuki, Y
Citation: T. Ogata et al., Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation, AM J MED G, 92(4), 2000, pp. 256-259
Authors:
Matsuo, M
Muroya, K
Nanao, K
Hasegawa, Y
Terasaki, H
Kosaki, K
Ogata, T
Citation: M. Matsuo et al., Mother and daughter with 45,X/46,X,r(X) (p22.3q28) and mental retardation:Analysis of the X-inactivation patterns, AM J MED G, 91(4), 2000, pp. 267-272
Authors:
Ogata, T
Muroya, K
Sasagawa, I
Kosho, T
Wakui, K
Sakazume, S
Ito, K
Matsuo, N
Ohashi, H
Nagai, T
Citation: T. Ogata et al., Genetic evidence for a novel gene(s) involved in urogenital development on10q26, KIDNEY INT, 58(6), 2000, pp. 2281-2290
Authors:
Obara, K
Muroya, K
Eguchi, K
Panli, Y
Citation: K. Obara et al., Angle dependence of transmission probability of incident electrons into thin oxide films and noise spectra, THIN SOL FI, 375(1-2), 2000, pp. 275-279
Authors:
Muroya, K
Okuyama, T
Goishi, K
Ogiso, Y
Fukuda, S
Kameyama, J
Sato, H
Suzuki, Y
Terasaki, H
Gomyo, H
Wakui, K
Fukushima, Y
Ogata, T
Citation: K. Muroya et al., Sex-determining gene(s) on distal 9p: Clinical and molecular studies in six cases, J CLIN END, 85(9), 2000, pp. 3094-3100
Authors:
Fukami, M
Kirsch, S
Schiller, S
Richter, A
Benes, V
Franco, B
Muroya, K
Rao, E
Merker, S
Niesler, B
Ballabio, A
Ansorge, W
Ogata, T
Rappold, GA
Citation: M. Fukami et al., A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation, AM J HU GEN, 67(3), 2000, pp. 563-573
Authors:
Muroya, K
Ishii, T
Nakahori, Y
Asakura, Y
Tachibana, K
Masuno, M
Imaizumi, K
Tanaka, Y
Kawada, Y
Yukizane, S
Ogata, T
Citation: K. Muroya et al., Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: Molecular analysis in four patients, GENE CHROM, 25(1), 1999, pp. 40-45
Authors:
Miyata, O
Yamakawa, S
Muroya, K
Naito, T
Citation: O. Miyata et al., An efficient synthesis and selective reaction of N-substituted isothiazolidinium salts, HETEROCYCLE, 51(7), 1999, pp. 1513
Authors:
Matsuo, M
Muroya, K
Kosaki, K
Ishii, T
Fukushima, Y
Anzo, M
Ogata, T
Citation: M. Matsuo et al., Random x-inactivation in a girl with duplication Xp11.21-p21.3: Report of a patient and review of the literature, AM J MED G, 86(1), 1999, pp. 44-50
Authors:
Muroya, K
Kosho, T
Ogata, T
Matsuo, M
Citation: K. Muroya et al., Female carriers of Xp22.3 deletion including MRX locus, AM J MED G, 84(4), 1999, pp. 384-385