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American Journal of Human Genetics|December 19, 2003
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese familyHui Zhao, Ronghua Li, Qiuju Wang, et al.
American Journal of Human Genetics|October 24, 2003
Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cellsZhi Yang, Rachel Lau, Julien L Marcadier, et al.
American Journal of Human Genetics|September 25, 2003
An Alu transposition model for the origin and expansion of human segmental duplicationsJeffrey A Bailey, Ge Liu, Evan E Eichler
American Journal of Human Genetics|January 24, 2004
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and readingCatherine M Stein, James H Schick, H Gerry Taylor, et al.
American Journal of Human Genetics|January 24, 2004
Mutations within the MGC4607 gene cause cerebral cavernous malformationsC Denier, S Goutagny, P Labauge, et al.
American Journal of Human Genetics|January 31, 2004
Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing informationTasha E Fingerlin, Michael Boehnke, Gonçalo R Abecasis
American Journal of Human Genetics|December 1, 1992
Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphismD A Nielsen, M Dean, D Goldman
American Journal of Human Genetics|December 1, 1992
Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locusL D Spotila, L Sereda, D J Prockop
American Journal of Human Genetics|January 20, 2004
Are variants in the CAPN10 gene related to risk of type 2 diabetes? A quantitative assessment of population and family-based association studiesYiqing Song, Tianhua Niu, JoAnn E Manson, et al.
American Journal of Human Genetics|January 30, 2004
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Gonçalo R Abecasis, Rachel A Burt, Diana Hall, et al.
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