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