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Birth Defects Original Article Series|January 1, 1984
Collection and analysis of pedigree dataD E GoldgarGenomics|December 1, 1987
Genetic analysis of NF1: identification of close flanking markers on chromosome 17P R Fain, D F Barker, D E Goldgar, et al.Annals of Human Genetics|July 1, 1978
Characteristics of simple sibship variance tests for the detection of major loci and application to height, weight and spatial performanceP R FainCytogenetics and Cell Genetics|January 1, 1992
Third International Workshop on Human Chromosome 17 MappingP R FainActa Geneticae Medicae Et Gemellologiae|January 1, 1980
Utility of genetic markers in the study of human resemblanceW J Kimberling, D E GoldgarGenetic Epidemiology|January 1, 1995
Screening for linkage using a multipoint identity-by-descent methodC M Lewis, D E GoldgarJournal of Clinical and Experimental Neuropsychology|August 1, 1988
Evaluation of a typology of reading disabilityB U Watson, D E GoldgarGenetic Epidemiology|January 1, 1997
The performance of MIM in comparison with MAPMAKER/SIBS to detect QTLsY Y Shugart, D E GoldgarEuropean Journal of Human Genetics : EJHG|April 10, 1999
Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approachY Y Shugart, D E GoldgarAmerican Journal of Human Genetics|March 1, 1992
Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traitsD E Goldgar, R S OnikiPageof 10