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American Journal of Human Genetics|December 1, 1987
Globin gene-associated restriction-fragment-length polymorphisms in southern African peoplesM Ramsay, T JenkinsAmerican Journal of Human Genetics|January 1, 1988
A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease geneM R Hayden, J Hewitt, J J Wasmuth, et al.American Journal of Human Genetics|January 1, 1988
Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkageN J Cox, L Baker, R S SpielmanAmerican Journal of Human Genetics|January 1, 1988
Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal XqP Saviranta, M Lindlöf, A E Lehesjoki, et al.American Journal of Human Genetics|September 1, 1986
A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary diseaseM F Leppert, S J Hasstedt, T Holm, et al.American Journal of Human Genetics|October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomesM H Hofker, M I Skraastad, A A Bergen, et al.American Journal of Human Genetics|July 9, 2016
Human Y Chromosome Haplogroup N: A Non-trivial Time-Resolved Phylogeography that Cuts across Language FamiliesAnne-Mai Ilumäe, Maere Reidla, Marina Chukhryaeva, et al.American Journal of Human Genetics|July 9, 2016
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis PigmentosaAndrea Angius, Paolo Uva, Insa Buers, et al.American Journal of Human Genetics|August 1, 2017
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple SclerosisDespoina Manousaki, Tom Dudding, Simon Haworth, et al.American Journal of Human Genetics|November 1, 1987
Linkage of DNA probe B79a (D7S13) to cystic fibrosisB J Wainwright, L C Tsui, M Leppert, et al.Pageof 979