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The Western Journal of Medicine|October 1, 1991
Molecular genetics of retinitis pigmentosaD B Farber, J R Heckenlively, R S Sparkes, et al.Science (New York, N.Y.)|September 25, 1981
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocationL C Strong, V M Riccardi, R E Ferrell, et al.American Journal of Medical Genetics|December 1, 1982
A 15 leads to 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)E A Wulfsberg, R S Sparkes, I J Klisak, et al.Genomics|April 1, 1993
Localization of the gene-encoding upstream stimulatory factor (USF) to human chromosome 1q22-q23B H Shieh, R S Sparkes, R B Gaynor, et al.Human Genetics|January 1, 1984
Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variantsM W Andersen, V P Williams, M C Sparkes, et al.Clinical Orthopaedics and Related Research|November 1, 1984
Hereditary multiple exostoses. Report of a familyB F Crandall, L L Field, R S Sparkes, et al.Human Genetics|November 1, 1989
Tissue specificity of chromosomal rearrangements in ataxia-telangiectasiaT L Kojis, R R Schreck, R A Gatti, et al.British Journal of Haematology|March 1, 1984
Bone marrow transplantation from identical twins in the treatment of aplastic anaemia: implication for the pathogenesis of the diseaseR E Champlin, S A Feig, R S Sparkes, et al.Leukemia Research|January 1, 1991
Hybrid leukemia and the 5q-abnormalityG Sun, S Wormsley, R S Sparkes, et al.Human Genetics|January 1, 1979
Prominent acrocentric chromosome satellites in child patients with mental retardation or psychiatric disorders; no IQ-satellite size correlationS J Funderburk, I Goldenberg, I Klisak, et al.Pageof 72