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of 4
pro vyhledávání: '"Gjt Meerman"'
Publikováno v:
Scandinavian journal of gastroenterology, 38(Suppl. 239), 63-68. Informa Healthcare
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 38, 63-68. Taylor & Francis Group
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 38, 63-68. Taylor & Francis Group
Background: Inflammatory bowel disease (IBD) is a complex disorder with an aetiology that is onlypartly understood. Apart from environmental factors, inheritance contributes to IBD. Review: Family studies show an increased risk among family members o
Publikováno v:
Genetic epidemiology, 21, S308-S311. Wiley
The Genetic Analysis Workshop 12 genome scan data set for "strict" asthma in a Hutterite population was analyzed using haplotype sharing analysis (HSA), which tests for differences in mean length of haplotype sharing around each marker for pairs of c
Autor:
Francesco Testa, N Hemmrich, G. Van Camp, R Santoss, J. C. Kaplan, S. Ingvast, Kris Flothmann, Francesca Simonelli, E Paloma, Carel B. Hoyng, Michele D'Urso, Alessandra Maugeri, Andres Metspalu, Reshma Patel, Paula Jorge, C Wadelius, Roser Gonzàlez-Duarte, Shomi S. Bhattacharya, Han G. Brunner, A C Bird, J Tammur, F. P. M. Cremers, Gjt Meerman, Susana Balcells, Jean-Michel Rozet, Marianne Schwartz, Bhf Weber, Rando Allikmets
Publikováno v:
EUROPEAN JOURNAL OF HUMAN GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
European journal of human genetics
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
European Journal of Human Genetics, 10, 197-203
European Journal of Human Genetics, 10, 3, pp. 197-203
European Journal of Human Genetics, 10(3), 197-203. Nature Publishing Group
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
European journal of human genetics
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
European Journal of Human Genetics, 10, 197-203
European Journal of Human Genetics, 10, 3, pp. 197-203
European Journal of Human Genetics, 10(3), 197-203. Nature Publishing Group
Item does not contain fulltext Inherited retinal dystrophies represent the most important cause of vision impairment in adolescence, affecting approximately 1 out of 3000 individuals. Mutations of the photoreceptor-specific gene ABCA4 (ABCR) are a co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6684b3297602d0c73d8b7733d5e5dc
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=11694
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=11694
Autor:
Gjt Meerman, D.J.A. Sonneveld, H. J. Hoekstra, H. Schraffordt Koops, Rolf H. Sijmons, Dt Sleijfer, Michael Schaapveld, Wta van der Graaf
Publikováno v:
British Journal of Cancer
British Jounal of Cancer, 81(7), 1262-1267. Nature Publishing Group
British Jounal of Cancer, 81(7), 1262-1267. Nature Publishing Group
Geographic variations in testicular cancer incidence may be caused by differences in environmental factors, genetic factors, or both. In the present study, geographic patterns of age-adjusted testicular cancer incidence rates (IRs) in 12 provinces in