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American Journal of Human Genetics|February 1, 1997
A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophyG Weeda, E Eveno, I Donker, et al.American Journal of Human Genetics|February 1, 1997
Sequence variation at the phenylalanine hydroxylase gene in the British IslesL A Tyfield, A Stephenson, F Cockburn, et al.American Journal of Human Genetics|February 1, 1997
Short alleles revealed by PCR demonstrate no heterozygote deficiency at minisatellite loci D1S7, D7S21, and D12S11S Alonso, A Castro, I Fernández-Fernández, et al.American Journal of Human Genetics|February 1, 1997
A variant of Freeman-Sheldon syndrome maps to 11p15.5-pterP A Krakowiak, J R O'Quinn, J F Bohnsack, et al.American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.American Journal of Human Genetics|April 1, 1997
Different mechanisms underlie DNA instability in Huntington disease and colorectal cancerG M Goellner, D Tester, S Thibodeau, et al.American Journal of Human Genetics|November 1, 1996
Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3L Boghosian-Sell, D E Comings, J OverhauserAmerican Journal of Human Genetics|November 1, 1996
Glutaric aciduria type I in the Arab and Jewish communities in IsraelY Anikster, A Shaag, A Joseph, et al.American Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P HechtmanAmerican Journal of Human Genetics|November 1, 1996
Analysis of loss of inactive X chromosomes in interphase cellsJ Surrallés, P Jeppesen, H Morrison, et al.Pageof 979