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American Journal of Human Genetics|July 1, 1997
A linkage strategy for detection of human quantitative-trait loci. II. Optimization of study designs based on extreme sib pairs and generalized relative risk ratiosC Gu, D C RaoAmerican Journal of Human Genetics|April 10, 2002
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasiaEri Arikawa-Hirasawa, Alexander H Le, Ichizo Nishino, et al.American Journal of Human Genetics|April 10, 2002
Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancerAnnika Rökman, Tarja Ikonen, Eija H Seppälä, et al.American Journal of Human Genetics|May 1, 1984
A strategy to reveal high-frequency RFLPs along the human X chromosomeJ Aldridge, L Kunkel, G Bruns, et al.American Journal of Human Genetics|January 1, 1983
A sib-pair strategy for the use of restriction fragment length polymorphisms to study the mode of transmission of type II diabetesB K SuarezAmerican Journal of Human Genetics|September 1, 1983
Prenatal diagnosis of GM1 gangliosidosis by detection of galactosyl-oligosaccharides in amniotic fluid with high-performance liquid chromatographyT G Warner, A D Robertson, A K Mock, et al.American Journal of Human Genetics|March 1, 1983
Distribution of break points in human structural rearrangementsY Nakagome, T Matsubara, H FujitaAmerican Journal of Human Genetics|April 2, 2002
Genomic disorders on 22q11Heather E McDermid, Bernice E MorrowAmerican Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.American Journal of Human Genetics|March 23, 2002
A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypesFulvio Cruciani, Piero Santolamazza, Peidong Shen, et al.Pageof 980