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Clinical Genetics|June 1, 1988
A linkage study of the locus for X-linked Charcot-Marie-Tooth diseaseP Goonewardena, J Welihinda, M Anvret, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|May 7, 2002
APOE genotypes and disease severity in multiple sclerosisT Masterman, Z Zhang, D Hellgren, et al.Clinical Genetics|December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosaN Dahl, M Sundvall, U Pettersson, et al.Pediatric Research|November 14, 1997
Increased leptin messenger RNA and serum leptin levels in children with Prader-Willi syndrome and nonsyndromal obesityA C Lindgren, C Marcus, C Skwirut, et al.American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.American Journal of Human Genetics|October 11, 2001
Huntington disease phenocopy is a familial prion diseaseR C Moore, F Xiang, J Monaghan, et al.Journal of Medical Genetics|December 1, 1995
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyriaG Lundin, J Hashemi, Y Floderus, et al.Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.American Journal of Human Genetics|October 30, 1998
A Huntington disease-like neurodegenerative disorder maps to chromosome 20pF Xiang, E W Almqvist, M Huq, et al.Pageof 173