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American Journal of Human Genetics|January 3, 2001
Point mutations of the mtDNA control region in normal and neurodegenerative human brainsP F Chinnery, G A Taylor, N Howell, et al.American Journal of Human Genetics|April 20, 2001
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal originR Trappe, F Laccone, J Cobilanschi, et al.American Journal of Human Genetics|April 20, 2001
Transformation of sib-pair values for the Haseman-Elston methodD Wang, S Lin, R Cheng, et al.American Journal of Human Genetics|November 15, 2000
A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31L Pattison, Y J Crow, V J Deeble, et al.American Journal of Human Genetics|November 30, 2000
AT-rich palindromes mediate the constitutional t(11;22) translocationL Edelmann, E Spiteri, K Koren, et al.American Journal of Human Genetics|December 12, 2000
A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3A Leal, B Morera, Del Valle G, et al.American Journal of Human Genetics|March 1, 1975
Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretationsN C Bethlenfalvay, A G Motulsky, B Ringelhann, et al.American Journal of Human Genetics|March 1, 1975
Evidence for the inactivation of an X chromosome early in the development of the human femaleB R Migeon, J F KennedyAmerican Journal of Human Genetics|January 13, 2001
A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16N Lee, M J Daly, T Delmonte, et al.American Journal of Human Genetics|February 15, 2001
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionA Richards, M R Buddles, R L Donne, et al.Pageof 980