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American Journal of Human Genetics|December 1, 1995
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populationsA Figus, A Angius, G Loudianos, et al.American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.American Journal of Human Genetics|December 1, 1995
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait lociC A McKenzie, C Julier, T Forrester, et al.American Journal of Human Genetics|December 1, 1995
Discordant patterns of linkage disequilibrium of the peptide-transporter loci within the HLA class II regionW Klitz, J C Stephens, M Grote, et al.American Journal of Human Genetics|December 1, 1995
Evolution of haplotypes at the DRD2 locusC M Castiglione, A S Deinard, W C Speed, et al.American Journal of Human Genetics|December 1, 1995
Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidenceD Ford, D F Easton, J PetoAmerican Journal of Human Genetics|August 1, 1992
Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagenL T Smith, W Wertelecki, L M Milstone, et al.American Journal of Human Genetics|August 1, 1992
Isolation, characterization, and regional mapping of microclones from a human chromosome 21 microdissection libraryJ Yu, J Hartz, Y Xu, et al.American Journal of Human Genetics|August 1, 1992
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease casesR E Tanzi, G Vaula, D M Romano, et al.American Journal of Human Genetics|August 1, 1992
Further localization of X-linked hydrocephalus in the chromosomal region Xq28P J Willems, L Vits, P Raeymaekers, et al.Pageof 979