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Human Genetics|September 1, 1994
Identification of trisomy in Macaca fascicularis by fluorescence in situ hybridization with a human chromosome 13 DNA libraryO G Ward, R L Miller, E H Johnson, et al.Human Genetics|September 1, 1994
Population genetic characteristics of the D1S80 locus in seven human populationsR Deka, S DeCroo, L Jin, et al.Human Genetics|September 1, 1994
A long range restriction map spanning the myxoid liposarcoma breakpoint in the q13-14 region of human chromosome 12A Forus, P F Kools, E F Schoenmakers, et al.Human Genetics|September 1, 1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosaC Reig, J Antich, E Gean, et al.Human Genetics|June 1, 1997
alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesP Miniou, M Jeanpierre, D Bourc'his, et al.Human Genetics|June 1, 1997
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsiesS Bort, E Nelis, V Timmerman, et al.Human Genetics|June 1, 1997
Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patientsM A Pujana, L Martorell, V Volpini, et al.Human Genetics|October 1, 1993
A high-resolution cytogenetic map of human chromosome 12: localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridizationE Takahashi, K Koyama, A Hitomi, et al.Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.Human Genetics|October 1, 1993
A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) geneC Lázaro, A Gaona, G Xu, et al.Pageof 957