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