Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 10

Results: 11

Ovarian cancer of endometrioid type as part of the MSH6 gene mutation phenotype.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 529, doi. 10.1007/s100380200079
By:
- Suchy, J.;
- Kurzawski, G.;
- Jakubowska, A.;
- Lubiński, J.
Publication type:
Article
Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 505, doi. 10.1007/s100380200075
By:
- Iida, A.;
- Saito, S.;
- Sekine, A.;
- Mishima, C.;
- Kitamura, Y.;
- Kondo, K.;
- Harigae, S.;
- Osawa, S.;
- Nakamura, Y.
Publication type:
Article
Familial 14-Mb deletion at 21q11.2–q21.3 and variable phenotypic expression.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 511, doi. 10.1007/s100380200076
By:
- Wakui, K.;
- Toyoda, A.;
- Kubota, T.;
- Hidaka, E.;
- Ishikawa, M.;
- Katsuyama, T.;
- Sakaki, Y.;
- Hattori, M.;
- Fukushima, Y.
Publication type:
Article
Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 532, doi. 10.1007/s100380200080
By:
- Akiyama, F.;
- Tanaka, T.;
- Yamada, R.;
- Ohnishi, Y.;
- Tsunoda, T.;
- Maeda, S.;
- Takei, T.;
- Obara, W.;
- Ito, K.;
- Honda, K.;
- Uchida, K.;
- Tsuchiya, K.;
- Nitta, K.;
- Yumura, W.;
- Nihei, H.;
- Ujiie, T.;
- Nagane, Y.;
- Miyano, S.;
- Suzuki, Y.;
- Fujioka, Tomoaki
Publication type:
Article
Yfm1, a multicopy marker specific for the Y chromosome and beneficial for forensic, population, genetic, and spermatogenesis-related studies.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 523, doi. 10.1007/s100380200078
By:
- Ewis, A. A.;
- Lee, J. W.;
- Kuroki, Y.;
- Shinka, T.;
- Nakahori, Y.
Publication type:
Article
No intraindividual variation of disomy rate in sperm samples.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 539, doi. 10.1007/s100380200081
By:
- Amiel, A.;
- Bartoov, B.;
- Pevsner, D.;
- Sardos-Albertini, F.;
- Fejgin, M. D.
Publication type:
Article
Two families with Wilson disease in which siblings showed different phenotypes.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 543, doi. 10.1007/s100380200082
By:
- Takeshita, Y.;
- Shimizu, N.;
- Yamaguchi, Y.;
- Nakazono, H.;
- Saitou, M.;
- Fujikawa, Y.;
- Aoki, T.
Publication type:
Article
Molecular cloning and characterization of a novel human Rab (Rab2B) gene.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 548, doi. 10.1007/s100380200083
By:
- Ni, X.;
- Ma, Y.;
- Cheng, H.;
- Jiang, M.;
- Guo, L.;
- Ji, C.;
- Gu, S.;
- Cao, Y.;
- Xie, Y.;
- Mao, Y.
Publication type:
Article
Comparative study on deletions of the dystrophin gene in three Asian populations.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 552, doi. 10.1007/s100380200084
By:
- Lai, P.-S.;
- Takeshima, Y.;
- Adachi, K.;
- van Tran, K.;
- Nguyen, H. Thi;
- Low, P.-S.;
- Matsuo, M.
Publication type:
Article
Structural analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 517, doi. 10.1007/s100380200077
By:
- Lee, H.-H.;
- Niu, D.-M.;
- Lin, R.-W.;
- Chan, P.;
- Lin, C.-Y.
Publication type:
Article
A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 10, p. 556, doi. 10.1007/s100380200085
By:
- Okamoto, N.;
- Toribe, Y.;
- Nakajima, T.;
- Okinaga, T.;
- Kurosawa, K.;
- Nonaka, I.;
- Shimokawa, O.;
- Matsumoto, N.
Publication type:
Article