Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 11

Results: 12

Epidemiology of X-linked adrenoleukodystrophy in Japan.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 590, doi. 10.1007/s100380200090

By:

Takemoto, Y.;
Suzuki, Y.;
Tamakoshi, A.;
Onodera, O.;
Tsuji, S.;
Hashimoto, T.;
Shimozawa, N.;
Orii, T.;
Kondo, N.

Publication type:

Article

A high-density SNP map for the FRAX region of the X chromosome.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 567, doi. 10.1007/s100380200087

By:

Brightwell, G.;
Wycherley, R.;
Potts, G.;
Waghorn, A.

Publication type:

Article

Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 576, doi. 10.1007/s100380200088

By:

Saito, S.;
Iida, A.;
Sekine, A.;
Ogawa, C.;
Kawauchi, S.;
Higuchi, S.;
Nakamura, Y.

Publication type:

Article

Distribution of two HIV-1-resistant polymorphisms (SDF1-3′A and CCR2-64I alleles) in the Polish population.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 585, doi. 10.1007/s100380200089

By:

Lewandowska, M.;
Franciszkiewicz, K.;
Prokop, J.;
Ofori, H.;
Jagodzinski, P. P.

Publication type:

Article

SNP alleles in human disease and evolution.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 561, doi. 10.1007/s100380200086

By:

Shastry, B. S.

Publication type:

Article

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 594, doi. 10.1007/s100380200091

By:

Sudoyo, H.;
Suryadi, H.;
Lertrit, P.;
Pramoonjago, P.;
Lyrawati, D.;
Marzuki, S.

Publication type:

Article

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190 562 genetic variations in the human genome.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 605, doi. 10.1007/s100380200092

By:

Haga, H.;
Yamada, R.;
Ohnishi, Y.;
Nakamura, Y.;
Tanaka, T.

Publication type:

Article

Polymorphisms in the gene encoding phosphatidylserine-specific phospholipase A1 (PSPLA1).

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 611, doi. 10.1007/s100380200093

By:

Wang, J.;
Wen, X.-Y.;
Stewart, A. K.;
Hegele, R. A.

Publication type:

Article

Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes: genomic structure and seven polymorphisms of the FAP-1 gene.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 614, doi. 10.1007/s100380200094

By:

Yoshida, S.;
Harada, H.;
Nagai, H.;
Fukino, K.;
Teramoto, A.;
Emi, M.

Publication type:

Article

DNA polymorphisms in ITPA including basis of inosine triphosphatase deficiency.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 620, doi. 10.1007/s100380200095

By:

Cao, H.;
Hegele, R. A.

Publication type:

Article

Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 11, p. 623, doi. 10.1007/s100380200096

By:

Tan, E.;
Wu, H.;
Yong, R.;
Tan, S.;
Chang, J.;
Gan, L.;
Yap, E.

Publication type:

Article

Errata: J Hum Genet (2002) 47:131–135.

Published in:: 2002
Publication type:: Erratum