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American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.American Journal of Human Genetics|March 1, 1993
Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resourcesJ M Fletcher, K Evans, D Baillie, et al.American Journal of Human Genetics|February 1, 1993
A single major-gene defect underlying cardiac conotruncal malformations interferes with myocardial growth during embryonic development: studies in the CTD line of keeshond dogsD F Patterson, T Pexieder, W R Schnarr, et al.American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.American Journal of Human Genetics|May 1, 1993
Incidence and origin of "null" alleles in the (AC)n microsatellite markersD F Callen, A D Thompson, Y Shen, et al.American Journal of Human Genetics|May 1, 1993
Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysisK A Rack, P C Harris, A B MacCarthy, et al.American Journal of Human Genetics|May 1, 1993
Diverse growth hormone receptor gene mutations in Laron syndromeM A Berg, J Argente, S Chernausek, et al.American Journal of Human Genetics|January 1, 1977
The Lutheran and secretor loci: genetic linkage analysisM Lewis, H Kaita, B Chown, et al.American Journal of Human Genetics|January 1, 1977
G6PD Ube, a glucose-6-phosphate dehydrogenase variant found in four unrelated Japanese familiesK Nakashima, J Ono, S Abe, et al.American Journal of Human Genetics|January 1, 1977
Frequency of an electrophoretic variant of hair alpha keratin in human populationsD B Hrdy, H P Baden, L D Lee, et al.Pageof 979