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American Journal of Human Genetics|March 11, 2000
mtDNA affinities of the peoples of North-Central MexicoL D Green, J N Derr, A KnightAmerican Journal of Human Genetics|March 11, 2000
Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresisS Finnilä, I E Hassinen, L Ala-Kokko, et al.American Journal of Human Genetics|March 11, 2000
The trimmed-haplotype test for linkage disequilibriumC J MacLean, R B Martin, P C Sham, et al.American Journal of Human Genetics|March 11, 2000
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2E Virolainen, M Wessman, I Hovatta, et al.American Journal of Human Genetics|March 11, 2000
A recurrent expansion of a maternal allele with 36 CAG repeats causes Huntington disease in two sistersF Laccone, W ChristianAmerican Journal of Human Genetics|March 11, 2000
The transmission/disequilibrium test for linkage on the X chromosomeG Y Ho, J E Bailey-WilsonAmerican Journal of Human Genetics|March 21, 2000
Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1I Eisenbarth, K Beyer, W Krone, et al.American Journal of Human Genetics|March 21, 2000
Detection of chromosomal aberrations by a whole-genome microsatellite screenM J Rosenberg, D Vaske, C E Killoran, et al.American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.American Journal of Human Genetics|March 21, 2000
A new locus for autosomal recessive hypercholesterolemia maps to human chromosome 15q25-q26M Ciccarese, A Pacifico, G Tonolo, et al.Pageof 979