Works matching IS 03406717 AND DT 2004 AND VI 115 AND IP 3

Results: 16

Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 255

By:

Xu, Jianfeng;
Langefeld, Carl D.;
Zheng, S. Lilly;
Gillanders, Elizabeth M.;
Chang, Bao-li;
Isaacs, Sarah D.;
Williams, Adrienne H.;
Wiley, Kathy E.;
Dimitrov, Latchezar;
Meyers, Deborah A.;
Walsh, Patrick C.;
Trent, Jeffrey M.;
Isaacs, William B.

Publication type:

Article

Alan E. Guttmacher, Francis S. Collins, Jeffrey M. Drazen (eds): Genomic medicine: articles from the New England Journal of Medicine: Johns Hopkins University Press (2004), The New England Journal of Medicine, ISBN 0-8018-7979-5, paperback, £27.50.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 265

By:

Read, Andrew P.

Publication type:

Article

A resistin gene polymorphism is associated with body mass index in women.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 208

By:

Mattevi, Vanessa S.;
Zembrzuski, Verônica M.;
Hutz, Mara H.

Publication type:

Article

Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 185

By:

Anderson, Sylvia L.;
Ekstein, Josef;
Donnelly, Mary C.;
Keefe, Erin M.;
Toto, Nicole R.;
LeVoci, Lauretta A.;
Rubin, Berish Y.

Publication type:

Article

Mono-nucleotide repeats (MNRs): a neglected polymorphism for generating high density genetic maps in silico.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 213, doi. 10.1007/s00439-004-1135-5

By:

Cohen, Helit;
Danin-Poleg, Yael;
Cohen, Cyril J.;
Sprecher, Eli;
Darvasi, Ariel;
Kashi, Yechezkel

Publication type:

Article

Chromosome 17p12-q11 harbors susceptibility loci for systemic lupus erythematosus.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 230

By:

Johansson, Cecilia M.;
Zunec, Renata;
García, Mercedes A.;
Scherbarth, Hugo R.;
Tate, Guillermo A.;
Paira, Sergio;
Navarro, Sandra M.;
Perandones, Carlos E.;
Gamron, Susana;
Alvarellos, Alejandro;
Graf, Cesar E.;
Manni, Jorge;
Berbotto, Guillermo A.;
Palatnik, Simon A.;
Catoggio, Luis J.;
Battagliotti, Cristina G.;
Sebastiani, Gian Domenico;
Migliaresi, Sergio;
Galeazzi, Mauro;
Pons-Estel, Bernardo A.

Publication type:

Article

Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 221, doi. 10.1007/s00439-004-1130-x

By:

Wooding, Stephen;
Ostler, Christopher;
Prasad, B. V. Ravi;
Watkins, W. Scott;
Sung, Sandy;
Bamshad, Mike;
Jorde, Lynn B.

Publication type:

Article

Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypes.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 239, doi. 10.1007/s00439-004-1147-1

By:

Clavero, Sonia;
Pérez, Belén;
Rincón, Ana;
Ugarte, Magdalena;
Desviat, Lourdes R.

Publication type:

Article

Max Perutz (ed) I wish I’d make you angry earlier. Expanded edition (2003): Cold Spring Harbor Laboratory Press, ISBN 0-87969-674-5, paperback, £11.00.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 267

By:

Harper, Peter S.

Publication type:

Article

B. Wissinger, S. Kohl, U. Langenbeck (eds): Developments in ophthalmology vol 37: Genetics in ophthalmology: S. Karger AG, ISBN 8-8055-7578-5, hardcover, 160.00 Euros, 224 pages.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 264, doi. 10.1007/s00439-004-1150-6

By:

Black, G. C. M.

Publication type:

Article

Thomas von Zglinicki (ed) Aging at the molecular level (2003): Kluwer Academic Publishers, Dordrecht, Boston, London, ISBN 1-4020-1738-3, hardcover, 125.00 Euro, $138.00.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 268, doi. 10.1007/s00439-004-1159-x

By:

Hoehn, Holger

Publication type:

Article

Identification of a novel type 1 diabetes susceptibility gene, T-bet.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 177, doi. 10.1007/s00439-004-1146-2

By:

Sasaki, Yuka;
Ihara, Kenji;
Matsuura, Nobuo;
Kohno, Hitoshi;
Nagafuchi, Seiho;
Kuromaru, Ryuichi;
Kusuhara, Koichi;
Takeya, Ryu;
Hoey, Timothy;
Sumimoto, Hideki;
Hara, Toshiro

Publication type:

Article

A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 248, doi. 10.1007/s00439-004-1143-5

By:

Kim, J.-W.;
Nam, S.-H.;
Jang, K.-T.;
Lee, S.-H.;
Kim, C.-C.;
Hahn, S.-H.;
Hu, J. C.-C.;
Simmer, J. P.

Publication type:

Article

Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 191

By:

Meşe, Gülistan;
Londin, Eric;
Mui, Rickie;
Brink, Peter R.;
White, Thomas W.

Publication type:

Article

Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 200, doi. 10.1007/s00439-004-1151-5

By:

Rannan-Eliya, Sahan V.;
Taylor, Indira B.;
de Heer, I. Marieke.;
van den Ouweland, Ans M. W.;
Wall, Steven A.;
Wilkie, Andrew O. M.

Publication type:

Article

Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.

Published in:

Human Genetics, 2004, v. 115, n. 3, p. 263

By:

Lim, Han N.;
Berkovitz, Gary D.;
Hughes, Ieuan A.;
Hawkins, J. Ross

Publication type:

Article