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Annales De Genetique|January 1, 1997
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patientsT Bienvenu, M Adjiman, N Thiounn, et al.Nucleic Acids Research|February 25, 1983
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22)A de la Chapelle, G Lenoir, J Boué, et al.Cell|August 26, 1994
Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophyS L Roberds, F Leturcq, V Allamand, et al.Leukemia|December 22, 1999
Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocationsM Busson-Le Coniat, F Salomon-Nguyen, N Dastugue, et al.Human Molecular Genetics|December 1, 1996
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of IndiaF Piccolo, M Jeanpierre, F Leturcq, et al.Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.Annals of Neurology|August 1, 1997
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in TurkeyP Dinçer, F Leturcq, I Richard, et al.Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.Neurology|May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophyB Eymard, N B Romero, F Leturcq, et al.Neurology|March 17, 2000
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutationL Merlini, J C Kaplan, C Navarro, et al.Pageof 6