Results: 1-25 | 26-29
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
Risultati: 1-25 | 26-29