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American Journal of Human Genetics|March 7, 2002
Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spotNadine Puget, Sophie Gad, Laure Perrin-Vidoz, et al.American Journal of Human Genetics|March 1, 1981
Fluorescence spectroscopic studies of Huntington fibroblast membranesJ R Lakowicz, J R SheppardAmerican Journal of Human Genetics|November 1, 1984
First-trimester prenatal diagnosis of mucolipidosis II (I-cell disease) by chorionic biopsyL Poenaru, L Castelnau, Y Dumez, et al.American Journal of Human Genetics|November 1, 1981
Hereditary heat-labile hexosaminidase B: its implication for recognizing Tay-Sachs genotypesR Navon, J Nutman, R Kopel, et al.American Journal of Human Genetics|December 17, 2005
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3Bettina Lorenz-Depiereux, Anna Benet-Pages, Gertrud Eckstein, et al.American Journal of Human Genetics|December 21, 2005
Regression-based association analysis with clustered haplotypes through use of genotypesJung-Ying Tzeng, Chih-Hao Wang, Jau-Tsuen Kao, et al.American Journal of Human Genetics|October 27, 2009
Use of a modified alpha-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry diseaseYouichi Tajima, Ikuo Kawashima, Takahiro Tsukimura, et al.American Journal of Human Genetics|January 1, 1991
Fitting mixture distributions to phenylthiocarbamide (PTC) sensitivityP N Jones, G J McLachlanAmerican Journal of Human Genetics|January 1, 1991
A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosaC F Inglehearn, R Bashir, D H Lester, et al.American Journal of Human Genetics|January 1, 1991
Immunochemical studies of ferrochelatase protein: characterization of the normal and mutant protein in bovine and human protoporphyriaJ G Straka, H D Hill, J M Krikava, et al.Pageof 980