Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 6

Results: 8

Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 269, doi. 10.1007/s100380200038
By:
- Kanno, K.;
- Suzuki, Y.;
- Yang, X.;
- Yamada, A.;
- Aoki, Y.;
- Kure, S.;
- Matsubara, Y.
Publication type:
Article
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 275, doi. 10.1007/s100380200039
By:
- Tachikawa, M.;
- Nagai, Y.;
- Nakamura, K.;
- Kobayashi, K.;
- Fujiwara, T.;
- Han, H.-J.;
- Nakabayashi, Y.;
- Ichikawa, Y.;
- Goto, J.;
- Kanazawa, I.;
- Nakamura, Y.;
- Toda, T.
Publication type:
Article
Complete XY gonadal dysgenesis and aspects of the SRY genotype and gonadal tumor formation.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 279, doi. 10.1007/s100380200040
By:
- Uehara, S.;
- Hashiyada, M.;
- Sato, K.;
- Nata, M.;
- Funato, T.;
- Okamura, K.
Publication type:
Article
Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 285, doi. 10.1007/s100380200041
By:
- Iida, A.;
- Saito, S.;
- Sekine, A.;
- Mishima, C.;
- Kitamura, Y.;
- Kondo, K.;
- Harigae, S.;
- Osawa, S.;
- Nakamura, Y.
Publication type:
Article
Phylogeographic analysis of mtDNA variation in four ethnic populations from Yunnan Province: new data and a reappraisal.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 311, doi. 10.1007/s100380200042
By:
- Yao, Y.-G.;
- Zhang, Y.-P.
Publication type:
Article
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 319, doi. 10.1007/s100380200043
By:
- De Marco, P.;
- Calevo, M. Grazia;
- Moroni, A.;
- Arata, L.;
- Merello, E.;
- Finnell, R. H.;
- Zhu, H.;
- Andreussi, L.;
- Cama, A.;
- Capra, V.
Publication type:
Article
Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 325, doi. 10.1007/s100380200044
By:
- Guo, Z.;
- Inazu, A.;
- Yu, W.;
- Suzumura, T.;
- Okamoto, M.;
- Nohara, A.;
- Higashikata, T.;
- Sano, R.;
- Wakasugi, K.;
- Hayakawa, T.;
- Yoshida, K.;
- Suehiro, T.;
- Schmitz, G.;
- Mabuchi, H.
Publication type:
Article
Genomic structure and eight novel exonic polymorphisms of the human N-cadherin gene.
Published in:
Journal of Human Genetics, 2002, v. 47, n. 6, p. 330, doi. 10.1007/s100380200045
By:
- Harada, H.;
- Kimura, A.;
- Fukino, K.;
- Yasunaga, S.;
- Nishi, H.;
- Emi, M.
Publication type:
Article