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Muscle & Nerve. Supplement|April 12, 2013
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.Neuroscience|May 11, 2010
Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohortB Krischek, A Tajima, H Akagawa, et al.Genes, Chromosomes & Cancer|June 1, 1996
Identification of the chimeric protein product of the CBFB-MYH11 fusion gene in inv(16) leukemia cellsP P Liu, C Wijmenga, A Hajra, et al.Neuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.Human Molecular Genetics|December 1, 1993
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitJ C van Deutekom, C Wijmenga, E A van Tienhoven, et al.Neuromuscular Disorders : NMD|July 1, 1993
Linkage and apparent heterogeneity in proximal spinal muscular atrophiesJ M Cobben, H Scheffer, M De Visser, et al.Gastroenterology|December 13, 2000
Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genesT Müller, C Wijmenga, A D Phillips, et al.American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.Allergy|December 15, 2010
Gene expression analysis predicts insect venom anaphylaxis in indolent systemic mastocytosisM Niedoszytko, M Bruinenberg, J J van Doormaal, et al.European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 17, 2003
IL12B and IRF1 gene polymorphisms and susceptibility to celiac diseaseD Seegers, M E A Borm, M J van Belzen, et al.Pageof 12