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American Journal of Human Genetics|July 27, 1999
Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injectionC Danan, D Sternberg, A Van Steirteghem, et al.American Journal of Human Genetics|July 27, 1999
Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorderR Kirk, R A Furlong, W Amos, et al.American Journal of Human Genetics|July 27, 1999
Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22M Mangino, O Sanchez, I Torrente, et al.American Journal of Human Genetics|April 17, 1999
Analysis of alkaptonuria (AKU) mutations and polymorphisms reveals that the CCC sequence motif is a mutational hot spot in the homogentisate 1,2 dioxygenase gene (HGO)D Beltrán-Valero de Bernabé, F J Jimenez, R Aquaron, et al.American Journal of Human Genetics|April 17, 1999
Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeatT R Rebbeck, P W Kantoff, K Krithivas, et al.American Journal of Human Genetics|April 17, 1999
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levelsP Pajukanta, J D Terwilliger, M Perola, et al.American Journal of Human Genetics|May 20, 1999
Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzymeR Seppala, V P Lehto, W A GahlAmerican Journal of Human Genetics|May 20, 1999
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafnessM J Kovach, J P Lin, S Boyadjiev, et al.American Journal of Human Genetics|May 20, 1999
Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortionR S Ozen, B E Baysal, B Devlin, et al.American Journal of Human Genetics|May 20, 1999
Homozygosity mapping of the Achromatopsia locus in the PingelapeseJ D Winick, M L Blundell, B L Galke, et al.Pageof 979