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Blood|November 1, 1978
Linkage and gene localization of hereditary spherocytosis (HS)W J Kimberling, R A Taylor, R G Chapman, et al.Science (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.The International Journal of Neuroscience|October 1, 1985
Phenotype of adult familial dyslexia: reading of visually transformed texts and nonsense passagesK Gross-Glenn, D C Lewis, S D Smith, et al.Research Publications - Association for Research in Nervous and Mental Disease|January 1, 1988
Dyslexia subtypes: genetics, behavior, and brain imagingH A Lubs, S Smith, W Kimberling, et al.Journal of Medical Genetics|October 3, 1999
A new gene (DYX3) for dyslexia is located on chromosome 2T Fagerheim, P Raeymaekers, F E Tønnessen, et al.Science (New York, N.Y.)|July 24, 1970
Genetic polymorphisms of human mitochondrial glutamic oxaloacetic transaminaseR G Davidson, J A Cortner, M C Rattazzi, et al.Annales De Genetique|December 11, 1976
Duplication-deficiency of the short arm of chromosome 8 following artificial inseminationR G Weleber, R S Verma, W J Kimberling, et al.Muscle & Nerve|July 1, 1978
Late-onset X-linked recessive spinal and bulbar muscular atrophyS P Ringel, N S Lava, M M Treihaft, et al.Clinical Genetics|April 10, 2002
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.American Journal of Medical Genetics|July 9, 1999
X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28K Armfield, R Nelson, H A Lubs, et al.Pageof 7