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American Journal of Human Genetics|April 1, 1997
Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblastsE A Putnam, E S Park, C M Aalfs, et al.American Journal of Human Genetics|April 1, 1997
Mutation analysis of the HLA-H gene in Italian hemochromatosis patientsM Carella, L D'Ambrosio, A Totaro, et al.American Journal of Human Genetics|April 1, 1997
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxiaD H Geschwind, S Perlman, C P Figueroa, et al.American Journal of Human Genetics|April 1, 1997
X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26M Lagerström-Fermér, M Sundvall, E Johnsen, et al.American Journal of Human Genetics|April 1, 1997
Autism or atypical autism in maternally but not paternally derived proximal 15q duplicationE H Cook, V Lindgren, B L Leventhal, et al.American Journal of Human Genetics|February 1, 1997
Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequencesC Sachse, J Brockmöller, S Bauer, et al.American Journal of Human Genetics|February 1, 1997
A potential role for NF1 mRNA editing in the pathogenesis of NF1 tumorsA J Cappione, B L French, G R SkuseAmerican Journal of Human Genetics|February 1, 1997
Mutation analysis of BRCA1 and BRCA2 in a male breast cancer populationL S Friedman, S A Gayther, T Kurosaki, et al.American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.American Journal of Human Genetics|February 1, 1997
Estimating the age of alleles by use of intraallelic variabilityM Slatkin, B RannalaPageof 980