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Current Allergy and Asthma Reports|March 15, 2002
Genetic factors underlying gluten-sensitive enteropathyA S Peña, C WijmengaClinical Genetics|May 21, 2011
Celiac disease: moving from genetic associations to causal variantsB Hrdlickova, H-J Westra, L Franke, et al.The Journal of Heredity|June 21, 2003
Indirect molecular diagnosis of copper toxicosis in Bedlington terriers is complicated by haplotype diversityB van de Sluis, A T Peter, C WijmengaJournal of Internal Medicine|March 16, 2011
Shared genetics in coeliac disease and other immune-mediated diseasesJ Gutierrez-Achury, R Coutinho de Almeida, C WijmengaJournal of Medical Genetics|August 25, 2007
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypesP de Bie, P Muller, C Wijmenga, et al.The Journal of Heredity|November 4, 2005
The many faces of the copper metabolism protein MURR1/COMMD1P de Bie, B van de Sluis, L Klomp, et al.Clinical Neurology and Neurosurgery|March 1, 1993
Facioscapulohumeral muscular dystrophy: the impact of genetic researchO F Brouwer, C Wijmenga, R R Frants, et al.Journal of Medical Genetics|September 8, 2001
Defining the genetic contribution of type 2 diabetes mellitusJ van Tilburg, T W van Haeften, P Pearson, et al.Archives of Neurology|April 1, 1994
Facioscapulohumeral muscular dystrophy in early childhoodO F Brouwer, G W Padberg, C Wijmenga, et al.European Journal of Medical Research|July 30, 1999
Non-Indian childhood cirrhosisT Müller, B van de Sluis, W Müller, et al.Pageof 12