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Lancet (London, England)|August 3, 1991
Hereditary unstable DNA: a new explanation for some old genetic questions?G R Sutherland, E A Haan, E Kremer, et al.American Journal of Human Genetics|June 1, 1991
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markersR I Richards, Y Shen, K Holman, et al.American Journal of Human Genetics|May 1, 1993
Incidence and origin of "null" alleles in the (AC)n microsatellite markersD F Callen, A D Thompson, Y Shen, et al.Genomics|April 1, 1994
A linkage map of microsatellite markers on the human X chromosomeA Donnelly, H Kozman, A K Gedeon, et al.American Journal of Medical Genetics|July 15, 1994
Haplotype analysis at the FRAXA locus in the Japanese populationR I Richards, I Kondo, K Holman, et al.Journal of Medical Genetics|December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile siteR I Richards, K Holman, H Kozman, et al.American Journal of Human Genetics|August 1, 1992
Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosomeJ T Clarke, P J Wilson, C P Morris, et al.Journal of Medical Genetics|March 1, 1997
Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal diseaseK Narahara, E Baker, S Ito, et al.American Journal of Human Genetics|August 1, 1993
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studiesI Aksentijevich, E Pras, L Gruberg, et al.American Journal of Human Genetics|September 1, 1993
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysisI Aksentijevich, E Pras, L Gruberg, et al.Pageof 57