Works matching IS 10184813 AND DT 2005 AND VI 13 AND IP 7

Results: 19

Hereditary hearing loss—the updated resource book more needed than ever.

Published in:

2005

By:

Tranebjærg, Lisbeth

Publication type:

Book Review

Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 840, doi. 10.1038/sj.ejhg.5201410

By:

Salanti, Georgia;
Amountza, Georgia;
Ntzani, Evangelia E.;
Ioannidis, John P. A.

Publication type:

Article

Genetic nephrology.

Published in:

2005

By:

Rusu, Cristina

Publication type:

Book Review

High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 856, doi. 10.1038/sj.ejhg.5201390

By:

Sanchez, Juan J.;
Hallenberg, Charlotte;
Børsting, Claus;
Hernandez, Alexis;
Morling, Niels

Publication type:

Article

Genetic Epidemiology.

Published in:

2005

By:

Stoll, Claude

Publication type:

Book Review

Association between SLC11A1 (formerly NRAMP1) and the risk of sarcoidosis in Poland.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 829, doi. 10.1038/sj.ejhg.5201370

By:

Dubaniewicz, Anna;
Jamieson, Sarra E.;
Dubaniewicz-Wybieralska, M.;
Fakiola, Michaela;
Nancy Miller, E.;
Blackwell, Jenefer M.

Publication type:

Article

Genetic stratification of pathogen-response-related and other variants within a homogeneous Caucasian Irish population.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 798, doi. 10.1038/sj.ejhg.5201382

By:

Dolan, Ciara;
O'Halloran, Aisling;
Bradley, Daniel G.;
Croke, David T.;
Evans, Alun;
O'Brien, John K.;
Dicker, Patrick;
Shields, Denis C.

Publication type:

Article

Complex Disease: A new vision for age-related macular degeneration.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 793, doi. 10.1038/sj.ejhg.5201431

By:

Gorin, Michael B.

Publication type:

Article

Contrasting patterns of Y chromosome and mtDNA variation in Africa: evidence for sex-biased demographic processes.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 867, doi. 10.1038/sj.ejhg.5201408

By:

Wood, Elizabeth T.;
Stover, Daryn A.;
Ehret, Christopher;
Destro-Bisol, Giovanni;
Spedini, Gabriella;
McLeod, Howard;
Louie, Leslie;
Bamshad, Mike;
Strassmann, Beverly I.;
Soodyall, Himla;
Hammer, Michael F.

Publication type:

Article

An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 807, doi. 10.1038/sj.ejhg.5201418

By:

Shengying Qin;
Xu Zhao;
Yuxi Pan;
Jianhua Liu;
Guoyin Feng;
Jingchun Fu;
Jiying Bao;
Zhizhou Zhang;
Lin He

Publication type:

Article

Association of DLG5 R30Q variant with inflammatory bowel disease.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 835, doi. 10.1038/sj.ejhg.5201403

By:

Daly, Mark J.;
Pearce, Alexandra V.;
Farwell, Lisa;
Fisher, Sheila A.;
Latiano, Anna;
Prescott, Natalie J.;
Forbes, Alastair;
Mansfield, John;
Sanderson, Jeremy;
Langelier, Diane;
Cohen, Albert;
Bitton, Alain;
Wild, Gary;
Lewis, Cathryn M.;
Annese, Vito;
Mathew, Christopher G.;
Rioux, John D.

Publication type:

Article

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 849, doi. 10.1038/sj.ejhg.5201413

By:

Holmkvist, Johan;
Almgren, Peter;
Parikh, Hemang;
Zucchelli, Marco;
Kere, Juha;
Groop, Leif;
Lindgren, Cecilia M.

Publication type:

Article

Association of the CTLA-4 gene with rheumatoid arthritis in Chinese Han population.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 823, doi. 10.1038/sj.ejhg.5201423

By:

Cai Lei;
Zhang Dongqing;
Shi Yeqing;
Oaks, Martin K.;
Chen Lishan;
Jin Jianzhong;
Qian Jie;
Du Fang;
Li Ningli;
Han Xinghai;
Ren DaMing

Publication type:

Article

An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 815, doi. 10.1038/sj.ejhg.5201422

By:

Bugeja, Matthew J.;
Booth, David R.;
Bennetts, Bruce H.;
Heard, Robert N. S.;
Burgner, David;
Stewart, Graeme J.

Publication type:

Article

TaqIB polymorphism in CETP gene: the influence on incidence of cardiovascular disease in statin-treated patients with familial hypercholesterolemia.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 877, doi. 10.1038/sj.ejhg.5201426

By:

Mohrschladt, Martina F.;
Van Der Sman-de Beer, Femke;
Hofman, Maaike K.;
van Der Krabben, Marieke;
Westendorp, Rudi G. J.;
Smelt, August H. M.

Publication type:

Article

A classic genetic text about classic genetic texts.

Published in:

2005

By:

Morrison, Patrick J.

Publication type:

Book Review

X Chromosome Inactivation: No longer ‘all-or-none’.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 796, doi. 10.1038/sj.ejhg.5201443

By:

Lyon, Mary F.

Publication type:

Article

Childhood overgrowth in patients with common NF1 microdeletions.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 883, doi. 10.1038/sj.ejhg.5201419

By:

Spiegel, Miriam;
Oexle, Konrad;
Horn, Denise;
Windt, Elke;
Buske, Annegret;
Albrecht, Beate;
Prott, Eva-Christina;
Seemanová, Eva;
Seidel, Joerg;
Rosenbaum, Thorsten;
Jenne, Dieter;
Kehrer-Sawatzki, Hildegard;
Tinschert, Sigrid

Publication type:

Article

Immunogenetics: Safety in numbers.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 795, doi. 10.1038/sj.ejhg.5201434

By:

Melief, Cornelis J. M.

Publication type:

Article