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American Journal of Medical Genetics|January 1, 1986
Variability of thymidylate synthase activity in whole blood cultures treated with FUdRS L Sklower, E C Jenkins, M L Anderson, et al.American Journal of Medical Genetics|January 1, 1986
Frequency of tri- or multiradial configurations in fragile X identificationE C Jenkins, C J Duncan, M S Krawczun, et al.American Journal of Medical Genetics|February 1, 1987
Attitudes of persons at risk for Huntington disease toward predictive testingS Kessler, T Field, L Worth, et al.American Journal of Medical Genetics|February 1, 1987
Attitudes toward presymptomatic testing in Huntington diseaseC Mastromauro, R H Myers, B BerkmanAmerican Journal of Medical Genetics|February 1, 1987
Intended use of predictive testing by those at risk for Huntington diseaseG J Meissen, R L BerchekAmerican Journal of Medical Genetics|October 1, 1986
Risk for trisomy 21 in offspring of individuals who have relatives with trisomy 21D Abuelo, G Barsel-Bowers, W Busch, et al.American Journal of Medical Genetics|January 15, 1992
Noninactivation of a portion of Xq28 in a balanced X-autosome translocationD Du Sart, P Kalitsis, M SchmidtAmerican Journal of Medical Genetics|January 15, 1992
Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)A Verloes, Y Gillerot, E Walczak, et al.American Journal of Medical Genetics|August 1, 1990
Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18G N Wilson, K B Heller, R D Elterman, et al.American Journal of Medical Genetics|September 1, 1991
Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative diseaseH L Grierson, J Skare, J Hawk, et al.Pageof 854