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American Journal of Human Genetics|March 21, 2000
Haplotype fine mapping by evolutionary treesJ C Lam, K Roeder, B Devlin
American Journal of Human Genetics|March 21, 2000
Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analysesT L Petryshen, B J Kaplan, M F Liu, et al.
American Journal of Human Genetics|March 21, 2000
Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtelM Topçu, C Gartioux, F Ribierre, et al.
American Journal of Human Genetics|January 13, 2000
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10S M van der Maarel, G Deidda, R J Lemmers, et al.
American Journal of Human Genetics|January 13, 2000
Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3M Ghadami, Y Makita, K Yoshida, et al.
American Journal of Human Genetics|January 13, 2000
The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14D Li, F Ahmad, M J Gardner, et al.
American Journal of Human Genetics|January 13, 2000
Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?J S Palmer, D L Duffy, N F Box, et al.
American Journal of Human Genetics|January 13, 2000
The number of trait loci in late-onset Alzheimer diseaseE W Daw, H Payami, E J Nemens, et al.
American Journal of Human Genetics|January 13, 2000
Laws restricting health insurers' use of genetic information: impact on genetic discriminationM A Hall, S S Rich
American Journal of Human Genetics|August 12, 1999
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutationsU Radhakrishna, D Bornholdt, H S Scott, et al.
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