Works matching IS 03406717 AND DT 2009 AND VI 124 AND IP 6

Results: 10

The joint association between F5 gene polymorphisms and maternal smoking during pregnancy on preterm delivery.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 659, doi. 10.1007/s00439-008-0589-2

By:

Yunxian Yu;
Hui-Ju Tsai;
Xin Liu;
Mestan, Karen;
Shanchun Zhang;
Pearson, Colleen;
Ortiz, Katherin;
Xiping Xu;
Zuckerman, Barry;
Xiaobin Wang

Publication type:

Article

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 649, doi. 10.1007/s00439-008-0588-3

By:

Daoud, Hussein;
Gruchy, Nicolas;
Constans, Jean-Marc;
Moussaoui, Edgar;
Saumureau, Simone;
Bayou, Nadia;
Amy, Maïté;
Védrine, Sylviane;
Phi Yen Vu;
Rötig, Agnès;
Laumonnier, Frédéric;
Vourc'h, Patrick;
Andres, Christian R.;
Leporrier, Nathalie;
Briault, Sylvain

Publication type:

Article

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

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 625, doi. 10.1007/s00439-008-0586-5

By:

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

Publication type:

Article

Advances in osteoclast biology resulting from the study of osteopetrotic mutations.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 561, doi. 10.1007/s00439-008-0583-8

By:

Segovia-Silvestre, T.;
Neutzsky-Wulff, A. V.;
Sorensen, M. G.;
Christiansen, C.;
Bollerslev, J.;
Karsdal, M. A.;
Henriksen, K.

Publication type:

Article

Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 593, doi. 10.1007/s00439-008-0582-9

By:

Pankratz, Nathan;
Wilk, Jemma B.;
Latourelle, Jeanne C.;
DeStefano, Anita L.;
Halter, Cheryl;
Pugh, Elizabeth W.;
Doheny, Kimberly F.;
Gusella, James F.;
Nichols, William C.;
Foroud, Tatiana;
Myers, Richard H.

Publication type:

Article

Lactose digestion and the evolutionary genetics of lactase persistence.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 579, doi. 10.1007/s00439-008-0593-6

By:

Ingram, Catherine J. E.;
Mulcare, Charlotte A.;
Itan, Yuval;
Thomas, Mark G.;
Swallow, Dallas M.

Publication type:

Article

A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 607, doi. 10.1007/s00439-008-0584-7

By:

Costas, Javier;
Carrera, Noa;
Domínguez, Eduardo;
Vilella, Elisabet;
Martorell, Lourdes;
Valero, Joaquín;
Gutiérrez-Zotes, Alfonso;
Labad, Antonio;
Carracedo, Ángel

Publication type:

Article

A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 615, doi. 10.1007/s00439-008-0585-6

By:

Adegbola, Abidemi A.;
Gonzales, Michael L.;
Chess, Andrew;
LaSalle, Janine M.;
Cox, Gerald F.

Publication type:

Article

Increased constraints on MC4R during primate and human evolution.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 633, doi. 10.1007/s00439-008-0591-8

By:

Hughes, David A.;
Hinney, Anke;
Brumm, Harald;
Wermter, Anne-Kathrin;
Biebermann, Heike;
Hebebrand, Johannes;
Stoneking, Mark

Publication type:

Article

A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2–q12.3.

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 669, doi. 10.1007/s00439-008-0596-3

By:

Chatterjee, Arunima;
Jalvi, Rajeev;
Pandey, Nishtha;
Rangasayee, R.;
Anand, Anuranjan

Publication type:

Article