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American Journal of Human Genetics|May 3, 2008
A defect in the TUSC3 gene is associated with autosomal recessive mental retardationMasoud Garshasbi, Valeh Hadavi, Haleh Habibi, et al.American Journal of Human Genetics|February 11, 1999
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the NetherlandsP Rizzu, J C Van Swieten, M Joosse, et al.American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.American Journal of Human Genetics|February 11, 1999
DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation ratesT Anagnostopoulos, P M Green, G Rowley, et al.American Journal of Human Genetics|February 11, 1999
Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1qM R Hobbs, A R Pole, G N Pidwirny, et al.American Journal of Human Genetics|February 11, 1999
Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22L Zu, K P Figueroa, R Grewal, et al.American Journal of Human Genetics|February 11, 1999
Congenital motor nystagmus linked to Xq26-q27J B Kerrison, M R Vagefi, M M Barmada, et al.American Journal of Human Genetics|February 11, 1999
The central Siberian origin for native American Y chromosomesF R Santos, A Pandya, C Tyler-Smith, et al.Pageof 979