Showing results (1331-1340 of 9,790) with videos related to
Sort By:
Pageof 979
American Journal of Human Genetics|February 17, 2001
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with ageJ L Elson, D C Samuels, D M Turnbull, et al.American Journal of Human Genetics|August 5, 2000
Identification and analysis of error types in high-throughput genotypingK R Ewen, M Bahlo, S A Treloar, et al.American Journal of Human Genetics|August 5, 2000
Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere additionH Varley, S Di, S W Scherer, et al.American Journal of Human Genetics|August 5, 2000
Familial aggregation of absolute pitchS Baharloo, S K Service, N Risch, et al.American Journal of Human Genetics|August 23, 2000
A novel nemaline myopathy in the Amish caused by a mutation in troponin T1J J Johnston, R I Kelley, T O Crawford, et al.American Journal of Human Genetics|August 12, 1999
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disordersY Liu, J Björkman, A Urquhart, et al.American Journal of Human Genetics|August 12, 1999
Missense mutation in the alternative splice region of the PAX6 gene in eye anomaliesN Azuma, Y Yamaguchi, H Handa, et al.American Journal of Human Genetics|August 12, 1999
Penetrances of BRCA1 1675delA and 1135insA with respect to breast cancer and ovarian cancerA Dørum, K Heimdal, E Hovig, et al.American Journal of Human Genetics|August 12, 1999
Polymorphic X-chromosome inactivation of the human TIMP1 geneC L Anderson, C J BrownAmerican Journal of Human Genetics|August 12, 1999
A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneityE Reid, A M Dearlove, M Rhodes, et al.Pageof 979