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Annals of Human Genetics|August 14, 2003
Y chromosome and mitochondrial DNA characterization of Pasiegos, a human isolate from Cantabria (Spain)N Maca-Meyer, P Sánchez-Velasco, C Flores, et al.Annals of Human Genetics|August 14, 2003
Assessing optimal neural network architecture for identifying disease-associated multi-marker genotypes using a permutation test, and application to calpain 10 polymorphisms associated with diabetesB V North, D Curtis, P G Cassell, et al.Annals of Human Genetics|August 14, 2003
Qualitative semi-parametric test for genetic associations in case-control designs under structured populationsH-S Chen, X Zhu, H Zhao, et al.Annals of Human Genetics|August 14, 2003
Smith-Lemli-Opitz syndrome and the DHCR7 geneP E Jira, H R Waterham, R J A Wanders, et al.Annals of Human Genetics|October 1, 1984
DNA analysis in patients with hereditary fructose intoleranceC Grégori, C Besmond, M Odievre, et al.Annals of Human Genetics|October 1, 1984
Fetal death rates in mothers of children with trisomy 21 (Down syndrome)A Lippman, S AyméAnnals of Human Genetics|January 1, 1978
The role of kin-structured migration in genetic microdifferentiationA G FixAnnals of Human Genetics|October 1, 1981
Regulation of expression of liver-specific enzymes. I. Detection in mammalian tissues and cultured cellsC M Kielty, S Povey, D A HopkinsonAnnals of Human Genetics|January 1, 1980
Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16S Povey, S J Jeremiah, R F Barker, et al.Annals of Human Genetics|May 1, 1994
Frequent normal allele loss and maternal origin of the mutation shown by DNA homoduplex analysis in a severely affected patient with adenomatous polyposis coliS A Gayther, M Rees, J D DelhantyPageof 231