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Somatic Cell and Molecular Genetics|July 1, 1991
Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase geneM E MacDonald, H S Scott, W L Whaley, et al.Nature Genetics|March 1, 1995
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3P L Tavormina, R Shiang, L M Thompson, et al.Genome Research|September 1, 1995
Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotationR G Del Mastro, L Wang, A D Simmons, et al.Human Molecular Genetics|March 1, 1993
The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA libraryR G Snell, L A Doucette-Stamm, K M Gillespie, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brainC M Ahmed, D H Ware, S C Lee, et al.American Journal of Human Genetics|March 3, 1999
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 geneP L Tavormina, G A Bellus, M K Webster, et al.Genome Research|October 6, 1997
A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript mapsJ D McPherson, B Apostol, C B Wagner-McPherson, et al.HIV Medicine|June 6, 2024
Clinical characteristics of women with HIV in the RESPOND cohort: A descriptive analysis and comparison to menJ Hutchinson, B Neesgard, J Kowalska, et al.Pageof 15