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Cytogenetic and Genome Research|August 12, 2004
Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndromeM Tadin-Strapps, D Warburton, F A M Baumeister, et al.Genomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.Experimental Dermatology|April 20, 2000
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesionsV M Aita, W Ahmad, A A Panteleyev, et al.European Journal of Human Genetics : EJHG|June 15, 2000
Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardationS Ranta, Y Zhang, B Ross, et al.Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 1, 1995
Genetic alterations of microsatellites on chromosome 18 in human breast carcinomaT H Huang, P L Yeh, M B Martin, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1988
Chromosome jumping from D4S10 (G8) toward the Huntington disease geneJ E Richards, T C Gilliam, J L Cole, et al.Neurology|September 1, 1991
Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locusP W Kleyn, L M Brzustowicz, K C Wilhelmsen, 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|September 1, 1991
Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13L L Lien, F M Boyce, P Kleyn, et al.Human Molecular Genetics|August 1, 1993
High resolution physical map of the region surrounding the spinal muscular atrophy geneT G Thompson, K E Morrison, P Kleyn, et al.Pageof 7