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American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.American Journal of Human Genetics|February 11, 1999
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26H Ikeda, T Sasaki, T Yoshimoto, et al.American Journal of Human Genetics|February 11, 1999
Mapping of primary congenital lymphedema to the 5q35.3 regionA L Evans, G Brice, V Sotirova, et al.American Journal of Human Genetics|February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7M C Speer, J M Vance, J M Grubber, et al.American Journal of Human Genetics|February 11, 1999
Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutationY Gong, D Chitayat, B Kerr, et al.American Journal of Human Genetics|February 11, 1999
Power of association and linkage tests when the disease alleles are unobservedI P Tu, A S WhittemoreAmerican Journal of Human Genetics|May 1, 1997
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484A Torroni, M Petrozzi, L D'Urbano, et al.American Journal of Human Genetics|May 1, 1997
Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisisL Huopaniemi, A Rantala, E Tahvanainen, et al.American Journal of Human Genetics|May 1, 1997
A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1E C Engle, A E Castro, M E Macy, et al.American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.Pageof 979