Works matching IS 03406717 AND DT 2009 AND VI 125 AND IP 2

Results: 15

Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

Published in:

2009

By:

Connell, F. C.;
Ostergaard, P.;
Carver, C.;
Brice, G.;
Williams, N.;
Mansour, S.;
Mortimer, P. S.;
Jeffery, Steve;
Consortium, Lymphoedema

Publication type:

Correction Notice

Alan G. Cock, Donald R. Forsdyke: Treasure your exceptions. The science and life of William Bateson.

Published in:

2009

By:

Harper, Peter S.

Publication type:

Book Review

Population admixture associated with disease prevalence in the Boston Puerto Rican health study.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 199, doi. 10.1007/s00439-008-0612-7

By:

Chao-Qiang Lai;
Tucker, Katherine L.;
Choudhry, Shweta;
Parnell, Laurence D.;
Mattei, Josiemer;
García-Bailo, Bibiana;
Beckman, Kenny;
Burchard, Esteban González;
Ordovás, José M.

Publication type:

Article

Air pollution and mutations in the germline: are humans at risk?

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 119, doi. 10.1007/s00439-008-0613-6

By:

Somers, Christopher M.;
Cooper, David N.

Publication type:

Article

Non-random X chromosome inactivation in Aicardi syndrome.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 211, doi. 10.1007/s00439-008-0615-4

By:

Eble, Tanya N.;
Sutton, V. Reid;
Haleh Sangi-Haghpeykar;
Xiaoling Wang;
Weihong Jin;
Lewis, Richard A.;
Ping Fang;
Van den Veyver, Ignatia B.

Publication type:

Article

Alterations of ROBO1/DUTT1 and ROBO2 loci in early dysplastic lesions of head and neck: clinical and prognostic implications.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 189, doi. 10.1007/s00439-008-0610-9

By:

Ghosh, Susmita;
Ghosh, Amlan;
Maiti, Guru Prasad;
Alam, Neyaz;
Roy, Anup;
Roychoudhury, Susanta;
Panda, Chinmay Kumar

Publication type:

Article

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 131, doi. 10.1007/s00439-008-0592-7

By:

Little, Julian;
Higgins, Julian P. T.;
Ioannidis, John P. A.;
Moher, David;
Gagnon, France;
von Elm, Erik;
Khoury, Muin J.;
Cohen, Barbara;
Davey-Smith, George;
Grimshaw, Jeremy;
Scheet, Paul;
Gwinn, Marta;
Williamson, Robin E.;
Guang Yong Zou;
Hutchings, Kim;
Johnson, Candice Y.;
Tait, Valerie;
Wiens, Miriam;
Golding, Jean;
van Duijn, Cornelia

Publication type:

Article

Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 181, doi. 10.1007/s00439-008-0611-8

By:

Thomas, N. Simon;
Maloney, Viv;
Bryant, Victoria;
Shuwen Huang;
Brewer, Carole;
Lachlan, Katherine;
Jacobs, Patricia A.

Publication type:

Article

Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 153, doi. 10.1007/s00439-008-0608-3

By:

Talbert, Matthew E.;
Langefeld, Carl D.;
Ziegler, Julie;
Mychaleckyj, Josyf C.;
Haffner, Steven M.;
Norris, Jill M.;
Bowden, Donald W.

Publication type:

Article

Stewart Scherer: A short guide to the human genome.

Published in:

2009

By:

Read, Andrew P.

Publication type:

Book Review

A comprehensive evaluation of SNP genotype imputation.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 163, doi. 10.1007/s00439-008-0606-5

By:

Nothnagel, Michael;
Ellinghaus, David;
Schreiber, Stefan;
Krawczak, Michael;
Franke, Andre

Publication type:

Article

Identification of genomic regions contributing to etoposide-induced cytotoxicity.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 173, doi. 10.1007/s00439-008-0607-4

By:

Bleibel, Wasim K.;
Shiwei Duan;
Huang, R. Stephanie;
Kistner, Emily O.;
Shukla, Sunita J.;
Xiaolin Wu;
Badner, Judith A.;
Dolan, M. Eileen

Publication type:

Article

Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.

Published in:

Human Genetics, 2009, v. 125, n. 2, p. 217, doi. 10.1007/s00439-008-0619-0

By:

Crosslin, David R.;
Shah, Svati H.;
Nelson, Sarah C.;
Haynes, Carol S.;
Connelly, Jessica J.;
Gadson, Shera;
Goldschmidt-Clermont, Pascal J.;
Vance, Jeffery M.;
Rose, Jason;
Granger, Chris B.;
Seo, David;
Gregory, Simon G.;
Kraus, William E.;
Hauser, Elizabeth R.

Publication type:

Article

Professor Peter S. Harper: A short history of medical genetics.

Published in:

2009

By:

Young, Ian

Publication type:

Book Review

STREGA: a ‘How-To’ guide for reporting genetic associations.

Published in:

2009

By:

Hudson, Thomas J.;
Cooper, David N.

Publication type:

Editorial