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American Journal of Human Genetics|October 30, 1998
Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11M I Othman, S A Sullivan, G L Skuta, et al.American Journal of Human Genetics|October 30, 1998
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18qA L DeStefano, C T Baldwin, M Burzstyn, et al.American Journal of Human Genetics|October 30, 1998
mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New WorldY B Starikovskaya, R I Sukernik, T G Schurr, et al.American Journal of Human Genetics|January 1, 1996
Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidusS Rittig, G L Robertson, C Siggaard, et al.American Journal of Human Genetics|January 1, 1996
Molecular definition of red cell Rh haplotypes by tightly linked SphI RFLPsC H Huang, M E Reid, Y Chen, et al.American Journal of Human Genetics|January 1, 1996
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formationD J Wolff, A P Miller, D L Van Dyke, et al.American Journal of Human Genetics|January 1, 1996
Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesisB R Migeon, P Jeppesen, B S Torchia, et al.American Journal of Human Genetics|January 1, 1996
Influence of apolipoprotein E genotype on the transmission of Alzheimer disease in a community-based sampleG Jarvik, E B Larson, K Goddard, et al.American Journal of Human Genetics|January 1, 1996
Segregation analysis of continuous phenotypes by using higher sample momentsH Lee, D O StramAmerican Journal of Human Genetics|January 1, 1996
Analysis of a splice-site mutation in the sap-precursor gene of a patient with metachromatic leukodystrophyM Henseler, A Klein, M Reber, et al.Pageof 979