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American Journal of Human Genetics|August 1, 1995
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.American Journal of Human Genetics|August 1, 1995
Fragile X gene instability: anchoring AGGs and linked microsatellitesN Zhong, W Yang, C Dobkin, et al.American Journal of Human Genetics|August 1, 1995
Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography traitA W Liu, A V Delgado-Escueta, J M Serratosa, et al.American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.American Journal of Human Genetics|August 1, 1995
Chromosome 9p deletions in cutaneous malignant melanoma tumors: the minimal deleted region involves markers outside the p16 (CDKN2) geneS Puig, A Ruiz, C Lázaro, et al.American Journal of Human Genetics|August 1, 1995
HLA class II linkage disequilibrium and haplotype evolution in the Cayapa Indians of EcuadorE A Trachtenberg, H A Erlich, O Rickards, et al.American Journal of Human Genetics|August 1, 1995
Analysis of complex human genetic traits: an ordered-notation method and new tests for mode of inheritanceG ThomsonAmerican Journal of Human Genetics|September 1, 1995
Mutation of the PAX6 gene in patients with autosomal dominant keratitisF Mirzayans, W G Pearce, I M MacDonald, et al.American Journal of Human Genetics|September 1, 1995
The molecular basis of canavan (aspartoacylase deficiency) disease in European non-Jewish patientsA Shaag, Y Anikster, E Christensen, et al.American Journal of Human Genetics|September 1, 1995
The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian populationM A Maw, D R Allen-Powell, R J Goodey, et al.Pageof 979