Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 10

Results: 16

Tuberous sclerosis.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1065, doi. 10.1038/sj.ejhg.5201625

By:

Yates, John R. W.

Publication type:

Article

Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1074, doi. 10.1038/sj.ejhg.5201649

By:

Khajavi, Mehrdad;
Inoue, Ken;
Lupski, James R.

Publication type:

Article

Reply to Hochstenbach et al.

Published in:

2006

By:

Vermeesch, Joris Robert;
Rauch, Anita

Publication type:

Letter

No evidence for association of a European-specific chromosome 17 inversion with multiple sclerosis.

Published in:

2006

By:

Goris, An;
Maranian, Melanie;
Walton, Amie;
Tai Wai Yeo;
Ban, Maria;
Gray, Julia;
Compston, Alastair;
Sawcer, Stephen

Publication type:

Letter

Chromosome 5 and Parkinson disease.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1106, doi. 10.1038/sj.ejhg.5201666

By:

Foroud, Tatiana;
Pankratz, Nathan;
Martinez, Maria

Publication type:

Article

The downstream modulator of interferon-γ, STAT1 is not genetically associated to the Dutch coeliac disease population.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1120, doi. 10.1038/sj.ejhg.5201667

By:

Diosdado, Begoña;
Monsuur, Alienke J.;
Mearin, María Luisa;
Mulder, Chris;
Wijmenga, Cisca

Publication type:

Article

Syndrome identification based on 2D analysis software.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1082, doi. 10.1038/sj.ejhg.5201673

By:

Boehringer, Stefan;
Vollmar, Tobias;
Tasse, Christiane;
Wurtz, Rolf P.;
Gillessen-Kaesbach, Gabriele;
Horsthemke, Bernhard;
Wieczorek, Dagmar

Publication type:

Article

A breath of fresh air: Respiratory Genetics.

Published in:

2006

By:

Morrison, Patrick J.

Publication type:

Book Review

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1090, doi. 10.1038/sj.ejhg.5201674

By:

Rooms, Liesbeth;
Reyniers, Edwin;
Scheers, Stefaan;
van Luijk, Rob;
Wauters, Jan;
Van Aerschot, Leen;
Callaerts-Vegh, Zsuzsanna;
D'Hooge, Rudi;
Mengus, Gabrielle;
Davidson, Irwin;
Courtens, Winnie;
Kooy, R. Frank

Publication type:

Article

A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1097, doi. 10.1038/sj.ejhg.5201670

By:

Rendtorff, Nanna D.;
Mei Zhu;
Fagerheim, Toril;
Antal, Torben L.;
Jones, MaryPat;
Teslovich, Tanya M.;
Gillanders, Elizabeth M.;
Barmada, Michael;
Teig, Erik;
Trent, Jeffrey M.;
Friderici, Karen H.;
Stephan, Dietrich A.;
Tranebjærg, Lisbeth

Publication type:

Article

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1111, doi. 10.1038/sj.ejhg.5201675

By:

Amann-Zalcenstein, Daniela;
Avidan, Nili;
Kanyas, Kyra;
Ebstein, Richard P.;
Kohn, Yoav;
Hamdan, Adnan;
Ben-Asher, Edna;
Karni, Osnat;
Mujaheed, Muhammed;
Segman, Ronnen H.;
Maier, Wolfgang;
Macciardi, Fabio;
Beckmann, Jacques S.;
Lancet, Doron;
Lerer, Bernard

Publication type:

Article

Association of a 31 bp VNTR in the CBS gene with postload homocysteine concentrations in the Framingham Offspring Study.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1125, doi. 10.1038/sj.ejhg.5201677

By:

Lievers, Karin J. A.;
Kluijtmans, Leo A. J.;
Blom, Henk J.;
Wilson, Peter W.;
Selhub, Jacob;
Ordovas, Jose M.

Publication type:

Article

A balanced perspective of psychiatric genetics: Psychiatric Genetics and Genomics.

Published in:

2006

By:

Jennings, Barbara A.

Publication type:

Book Review

Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1130, doi. 10.1038/sj.ejhg.5201680

By:

Dawei Li;
Lin He

Publication type:

Article

DNA repair gene XRCC3 polymorphisms and cancer risk: a meta-analysis of 48 case–control studies.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1136, doi. 10.1038/sj.ejhg.5201681

By:

Shizhong Han;
Hong-Tao Zhang;
Zhentian Wang;
Yi Xie;
Tang, Rong;
Yumin Mao;
Yao Li

Publication type:

Article

Parkinson's Disease: The LRRK2-G2019S mutation: opening a novel era in Parkinson's disease genetics.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1061, doi. 10.1038/sj.ejhg.5201695

By:

Bonifati, Vincenzo

Publication type:

Article