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Journal of the Neurological Sciences|February 1, 1990
Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5C Wijmenga, R R Frants, O F Brouwer, et al.Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|August 29, 2009
Genetic variation in the hypothalamic pathways and its role on obesityJ V van Vliet-Ostaptchouk, M H Hofker, Y T van der Schouw, et al.Journal of Neurology|February 24, 2005
Genes and outcome after aneurysmal subarachnoid haemorrhageY M Ruigrok, A J C Slooter, A Bardoel, et al.American Journal of Human Genetics|October 1, 1995
Genetic mapping of the dentinogenesis imperfecta type II locusA H Crosby, T Scherpbier-Heddema, C Wijmenga, et al.Journal of Medical Genetics|January 1, 1996
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial casesE Bakker, M J Van der Wielen, E Voorhoeve, et al.Cytogenetics and Cell Genetics|July 28, 2001
Characterization and chromosomal localization of five canine ATOX1 pseudogenesB van de Sluis, M S Nanji, M Breen, et al.Muscle & Nerve. Supplement|January 1, 1995
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.European Journal of Clinical Investigation|November 26, 2003
Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch populationJ H van Tilburg, L A Sandkuijl, L Franke, et al.American Journal of Human Genetics|June 13, 1998
Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphroditeJ C Giltay, T Brunt, F A Beemer, et al.Pageof 12