Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 4

Results: 11

Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 281, doi. 10.1038/sj.ejhg.5200796

By:

Stohr, Heidi;
Marquardt, Andreas;
Nanda, Indrajit;
Schmid, Michael;
Weber, Bernhard H.F.

Publication type:

Article

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 276, doi. 10.1038/sj.ejhg.5200803

By:

Del-Favero, Jurgen;
Van Gestel, Sofie;
Borglum, Anders D.;
Muir, Walter;
Ewald, Henrik;
Mors, Ole;
Ivezic, Sladana;
Oruc, Lilijana;
Adolfsson, Rolf;
Blackwood, Douglas;
Kruse, Torben;
Mendlewicz, Julien;
Schalling, Martin;
Van Broeckhoven, Christine

Publication type:

Article

Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 271, doi. 10.1038/sj.ejhg.5200802

By:

He, Bing;
Giedraitis, Vilmantas;
Ligers, Arturs;
Binzer, Michael;
Andersen, Peter M.;
Forsgren, Lars;
Sandkuijl, Lodewijk A.;
Hillert, Jan

Publication type:

Article

Positive association to lgE levels and a physical map of the 13q14 atopy locus.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 266, doi. 10.1038/sj.ejhg.5200801

By:

Anderson, Gavin G.;
Leaves, Nicholas I.;
Bhattacharyya, Sumit;
Zhang, Youming;
Walshe, Valerie;
Broxholme, John;
Abecasis, Goncalo;
Levy, Elaine;
Zimmer, Michael;
Cox, Roger;
Cookson, William O.C.M.

Publication type:

Article

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 259, doi. 10.1038/sj.ejhg.5200792

By:

Fisher, Sheila A.;
Hampe, Jochen;
Macpherson, Andrew J.S.;
Forbes, Alastair;
Lennard-Jones, John E.;
Schreiber, Stefan;
Curran, Mark E.;
Mathew, Christopher G.;
Lewis, Cathryn M.

Publication type:

Article

Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 250, doi. 10.1038/sj.ejhg.5200798

By:

Popovic, Maja;
Goobie, Sharan;
Morrison, Jodi;
Ellis, Lynda;
Ehtesham, Nadia;
Richards, Nicole;
Boocock, Graeme;
Durie, Peter R.;
Rommens, Johanna M.

Publication type:

Article

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 245, doi. 10.1038/sj.ejhg.5200797

By:

Keen, T. Jeffrey;
Hims, Matthew M.;
McKie, Arthur B.;
Moore, Anthony T.;
Doran, Rob M.;
Mackey, David A.;
Mansfield, David C.;
Mueller, Robert F.;
Bhattacharya, Shomi S.;
Bird, Alan C.;
Markham, Alexander F.;
Inglehearn, Chris F.

Publication type:

Article

Analysis of alterations of WFDC1, a new putative tumor suppressor gene, in hepatocellular carcinoma.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 239, doi. 10.1038/sj.ejhg.5200795

By:

Saffroy, Raphael;
Riou, Philippe;
Soler, Gwendoline;
Azoulay, Daniel;
Emile, Jean-Francois;
Debuire, Brigitte;
Lemoine, Antoinette

Publication type:

Article

Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 230

By:

Moutou, Celine;
Gardes, Nathalie;
Viville, Stephane

Publication type:

Article

MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorder.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 226, doi. 10.1038/sj.ejhg.5200791

By:

Leshinsky-Silver, Esther;
Zinger, Ami;
Bibi, Chaim N.;
Barash, Varda;
Sadeh, Menachem;
Lev, Dorit;
Sagie, Tally Lerman

Publication type:

Article

Alpha-thalassemia/mental retardation syndrome, X-Linked (ATR-X, MIM #301040, ATR-X/XNP/XH2 gene MIM #30032.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 4, p. 223, doi. 10.1038/sj.ejhg.5200800

By:

Villard, Laurent;
Fontes, Michel

Publication type:

Article