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Journal of the American Academy of Child and Adolescent Psychiatry|March 1, 1990
Familial dyslexia: use of genetic linkage data to define subtypesS D Smith, B F Pennington, W J Kimberling, et al.Clinical Genetics|September 1, 1983
Cytogenetic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y;13) translocation showing differential centromeric activityP S Ing, S D SmithScience (New York, N.Y.)|March 18, 1983
Specific reading disability: identification of an inherited form through linkage analysisS D Smith, W J Kimberling, B F Pennington, et al.Archives of Neurology|June 1, 1987
Left-handedness and immune disorders in familial dyslexicsB F Pennington, S D Smith, W J Kimberling, et al.Journal of Communication Disorders|October 20, 1998
Medical genetic evaluation for the etiology of hearing loss in childrenS D Smith, W J Kimberling, G B Schaefer, et al.Genomics|December 28, 1999
Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12P M Kelley, S Abe, J W Askew, et al.Science (New York, N.Y.)|October 14, 1994
Quantitative trait locus for reading disability on chromosome 6L R Cardon, S D Smith, D W Fulker, et al.Journal of the American Academy of Audiology|January 1, 1995
Clinical and molecular genetics of Usher syndromeW J Kimberling, C MöllerScience (New York, N.Y.)|June 16, 1995
Quantitative trait locus for reading disability: correctionL R Cardon, S D Smith, D W Fulker, et al.Pageof 45