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American Journal of Human Genetics|February 1, 1996
A 10-bp deletion in the apolipoprotein epsilon gene causing apolipoprotein E deficiency and severe type III hyperlipoproteinemiaG Feussner, J Dobmeyer, H J Gröne, et al.
American Journal of Human Genetics|February 1, 1996
Gametogenesis processes and multilocus gene identity by descentS W Guo
American Journal of Human Genetics|May 1, 1993
A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease lociC W Richard, M Boehnke, D J Berg, et al.
American Journal of Human Genetics|June 1, 1993
Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second geneJ Wang, J Zhou, S M Todorovic, et al.
American Journal of Human Genetics|May 1, 1977
Characterization of a variant of beta-hexosaminidase: "hexosaminidase Paris"J C Dreyfus, L Poenaru, M Vibert, et al.
American Journal of Human Genetics|February 22, 2002
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive conditionHeidemarie Neitzel, Luitgard M Neumann, Detlev Schindler, et al.
American Journal of Human Genetics|February 15, 2002
The structure of diversity within New World mitochondrial DNA haplogroups: implications for the prehistory of North AmericaRipan S Malhi, Jason A Eshleman, Jonathan A Greenberg, et al.
American Journal of Human Genetics|December 31, 2005
Deletion of PREPL, a gene encoding a putative serine oligopeptidase, in patients with hypotonia-cystinuria syndromeJaak Jaeken, Kevin Martens, Inge Francois, et al.
American Journal of Human Genetics|December 31, 2005
Variants associated with common disease are not unusually differentiated in frequency across populationsKirk E Lohmueller, Matthew M Mauney, David Reich, et al.
American Journal of Human Genetics|October 30, 1998
Familial porphyria cutanea tarda: characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis allelesM Mendez, L Sorkin, M V Rossetti, et al.
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