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Genomics|December 1, 1994
A PCR-based genetic map for human chromosome 3P O'Connell, R J Leach, D Rains, et al.Nature Genetics|April 1, 1994
Localization of a gene causing cystinuria to chromosome 2pE Pras, N Arber, I Aksentijevich, et al.Journal of Medical Genetics|December 1, 1995
No evidence of genetic heterogeneity in dominant optic atrophyD Bonneau, E Souied, S Gerber, et al.Genome Research|May 1, 1996
Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8pS Ranta, A E Lehesjoki, A Hirvasniemi, et al.Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8E Tahvanainen, S Ranta, A Hirvasniemi, et al.Genomics|December 12, 2001
Homology between a 173-kb region from mouse chromosome 10, telomeric to the Ifng locus, and human chromosome 12q15S Vigneau, F Levillayer, H Crespeau, et al.Genomics|May 1, 1995
The CEPH consortium linkage map of human chromosome 11M Litt, P Kramer, E Kort, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigreesP De Jonghe, L Krols, A Michalik, et al.Genomics|December 1, 1994
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 lociC Graff, K Forsman, C Larsson, et al.Human Molecular Genetics|September 1, 1995
Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mappingS Nicole, C Ben Hamida, P Beighton, et al.Pageof 46