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American Journal of Human Genetics|June 23, 1998
Direct evidence for suppression of recombination within two pericentric inversions in humans: a new sperm-FISH techniqueM Jaarola, R H Martin, T AshleyAmerican Journal of Human Genetics|June 23, 1998
PedCheck: a program for identification of genotype incompatibilities in linkage analysisJ R O'Connell, D E WeeksAmerican Journal of Human Genetics|June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophyS Cacurri, N Piazzo, G Deidda, et al.American Journal of Human Genetics|June 23, 1998
Evidence that a locus for familial high myopia maps to chromosome 18pT L Young, S M Ronan, L A Drahozal, et al.American Journal of Human Genetics|June 23, 1998
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNAM G Hanna, I P Nelson, S Rahman, et al.American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.American Journal of Human Genetics|June 23, 1998
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteriaR Kruse, A Rütten, C Lamberti, et al.American Journal of Human Genetics|June 23, 1998
Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreportingS W GuoAmerican Journal of Human Genetics|June 23, 1998
The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097-->T transversion in NPC1W L Greer, D C Riddell, T L Gillan, et al.American Journal of Human Genetics|June 13, 1998
A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprintingC R Weinberg, A J Wilcox, R T LiePageof 979