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Developmental Medicine and Child Neurology|April 1, 1983
Regional cerebral glucose metabolism of newborn infants measured by positron emission tomographyL W Doyle, C Nahmias, G Firnau, et al.
Genomics|December 1, 1993
Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23W J Kimberling, S Kumar, P A Gabow, et al.
The New England Journal of Medicine|October 6, 1988
Linkage heterogeneity of autosomal dominant polycystic kidney diseaseW J Kimberling, P R Fain, J B Kenyon, et al.
The Laryngoscope|April 1, 1997
Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutationS Usami, S Abe, M Kasai, et al.
Cytogenetics and Cell Genetics|October 9, 1998
Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian familyK Kirschhofer, J B Kenyon, D M Hoover, et al.
Human Molecular Genetics|October 1, 1992
Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch familyS Kumar, W J Kimberling, J B Kenyon, et al.
JMIR Formative Research|July 20, 2023
Mobile Web App Intervention to Promote Breast Cancer Screening Among American Indian Women in the Northern Plains: Feasibility and Efficacy StudySoonhee Roh, Yeon-Shim Lee, DenYelle B Kenyon, et al.
American Journal of Human Genetics|October 23, 1997
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6pM R Brown, M S Tomek, L Van Laer, et al.
Human Genetics|May 13, 2004
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analysesKaren E Deffenbacher, Judith B Kenyon, Denise M Hoover, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutationS Abe, S Usami, H Shinkawa, et al.
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