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American Journal of Human Genetics|July 31, 1998
Association of MSX1 and TGFB3 with nonsyndromic clefting in humansA C Lidral, P A Romitti, A M Basart, et al.American Journal of Human Genetics|July 31, 1998
Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship dataL Abel, B Müller-MyhsokAmerican Journal of Human Genetics|July 31, 1998
Malaria in humans: Plasmodium falciparum blood infection levels are linked to chromosome 5q31-q33P Rihet, Y Traoré, L Abel, et al.American Journal of Human Genetics|July 31, 1998
Commitment to X inactivation precedes the twinning event in monochorionic MZ twinsJ Monteiro, C Derom, R Vlietinck, et al.American Journal of Human Genetics|July 31, 1998
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qterM Hirano, J Garcia-de-Yebenes, A C Jones, et al.American Journal of Human Genetics|July 31, 1998
Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13S M Wang, J Zwaan, P B Mullaney, et al.American Journal of Human Genetics|July 31, 1998
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase geneH R Waterham, F A Wijburg, R C Hennekam, et al.American Journal of Human Genetics|August 27, 1998
Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosisD G Evans, A J Wallace, C L Wu, et al.American Journal of Human Genetics|August 27, 1998
Evidence for at least two major loci influencing human fatnessI B Borecki, J Blangero, T Rice, et al.American Journal of Human Genetics|August 27, 1998
Evidence from human oocytes for a genetic bottleneck in an mtDNA diseaseD R Marchington, V Macaulay, G M Hartshorne, et al.Pageof 979