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Human Molecular Genetics|March 1, 1996
Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophyC H Wang, J Xu, T A Carter, et al.Human Heredity|November 1, 1993
Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophyL M Brzustowicz, C Mérette, P W Kleyn, et al.Genomics|February 1, 1993
Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1BV M Soares, L M Brzustowicz, P W Kleyn, et al.Genomics|January 1, 1993
A microsatellite genetic linkage map of human chromosome 13K E Petrukhin, M C Speer, E Cayanis, et al.Somatic Cell and Molecular Genetics|January 1, 1993
A genetic linkage map of the chromosome 4 short armP A Locke, M E MacDonald, J Srinidhi, et al.Genomics|May 1, 1994
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophyC Mérette, L M Brzustowicz, R J Daniels, et al.American Journal of Human Genetics|January 1, 1995
Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophyL M Brzustowicz, C H Wang, D Matseoane, et al.Nature|June 28, 1990
Genetic homogeneity between acute and chronic forms of spinal muscular atrophyT C Gilliam, L M Brzustowicz, L H Castilla, et al.Science (New York, N.Y.)|September 21, 1984
DNA markers for nervous system diseasesJ F Gusella, R E Tanzi, M A Anderson, et al.Annals of Neurology|February 1, 1991
Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosomeK C Wilhelmsen, D E Weeks, T G Nygaard, et al.Pageof 7