Works matching IS 03406717 AND DT 2009 AND VI 125 AND IP 3

Results: 12

Gene polymorphisms, apoptotic capacity and cancer risk.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 239, doi. 10.1007/s00439-009-0636-7

By:

Imyanitov, Evgeny N.

Publication type:

Article

Pyruvate dehydrogenase phosphatase 1 ( PDP1) null mutation produces a lethal infantile phenotype.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 319, doi. 10.1007/s00439-009-0629-6

By:

Cameron, J. M.;
Maj, M.;
Levandovskiy, V.;
Barnett, C. P.;
Blaser, S.;
MacKay, N.;
Raiman, J.;
Feigenbaum, A.;
Schulze, A.;
Robinson, B. H.

Publication type:

Article

Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 295, doi. 10.1007/s00439-009-0627-8

By:

Egyud, Matthew R. L.;
Gajdos, Zofia K. Z.;
Butler, Johannah L.;
Tischfield, Sam;
Le Marchand, Loic;
Kolonel, Laurence N.;
Haiman, Christopher A.;
Henderson, Brian E.;
Hirschhorn, Joel N.

Publication type:

Article

Charles J. Epstein, Robert P. Erickson, Anthony Wynshaw-Boris (eds): Inborn errors of development.

Published in:

2009

By:

Tolmie, John

Publication type:

Book Review

Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 305, doi. 10.1007/s00439-009-0626-9

By:

Bossé, Yohan;
Bacot, François;
Montpetit, Alexandre;
Johan Rung;
Hui-Qi Qu;
Engert, James C.;
Polychronakos, Constantin;
Hudson, Thomas J.;
Froguel, Philippe;
Sladek, Robert;
Desrosiers, Martin

Publication type:

Article

Association of Y chromosome haplogroup I with HIV progression, and HAART outcome.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 281, doi. 10.1007/s00439-008-0620-7

By:

Sezgin, Efe;
Lind, Joanne M.;
Shrestha, Sadeep;
Hendrickson, Sher;
Goedert, James J.;
Donfield, Sharyne;
Kirk, Gregory D.;
Phair, John P.;
Troyer, Jennifer L.;
O'Brien, Stephen J.;
Smith, Michael W.

Publication type:

Article

Dhavendra Kumar (ed): Genomics and clinical medicine.

Published in:

2009

By:

Donnai, Dian

Publication type:

Book Review

Analysis of the MTHFD1 promoter and risk of neural tube defects.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 247, doi. 10.1007/s00439-008-0616-3

By:

Carroll, Nicola;
Pangilinan, Faith;
Molloy, Anne M.;
Troendle, James;
Mills, James L.;
Kirke, Peadar N.;
Brody, Lawrence C.;
Scott, John M.;
Parle-McDermott, Anne

Publication type:

Article

Novel human pathological mutations.

Published in:

2009

By:

Martínez-Rubio, Dolores;
Millán, José;
Palau, Francesc;
Espinós, Carmen

Publication type:

Correction Notice

Huntington F. Willard and Geoffrey S. Ginsburg (eds): Genomic and personalized medicine.

Published in:

2009

By:

Cooper, David N.

Publication type:

Book Review

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 257, doi. 10.1007/s00439-008-0621-6

By:

Hodge, Jennelle C.;
Cuenco, Karen T.;
Huyck, Karen L.;
Somasundaram, Priya;
Panhuysen, Carolien I. M.;
Stewart, Elizabeth A.;
Morton, Cynthia C.

Publication type:

Article

New genetic evidence for involvement of the dopamine system in migraine with aura.

Published in:

Human Genetics, 2009, v. 125, n. 3, p. 265, doi. 10.1007/s00439-009-0623-z

By:

Todt, Unda;
Netzer, Christian;
Toliat, Mohammad;
Heinze, Axel;
Goebel, Ingrid;
Nürnberg, Peter;
Göbel, Hartmut;
Freudenberg, Jan;
Kubisch, Christian

Publication type:

Article