Showing results (1-10 of 111) with videos related to
Sort By:
Pageof 12
Mutation Research|November 1, 1979
G2 chromosomal radiosensitivity in Fanconi's anemiaS B Bigelow, J M Rary, M A BenderThe Journal of Heredity|January 1, 1975
A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasiaJ M Rary, M A Bender, T E KellyMutation Research|June 1, 1985
G0 chromosomal radiosensitivity in ataxia telangiectasia lymphocytesM A Bender, J M Rary, R P KaleMutation Research|October 1, 1985
G2 chromosomal radiosensitivity in ataxia telangiectasia lymphocytesM A Bender, J M Rary, R P KaleAmerican Journal of Medical Genetics|January 1, 1986
Speculation on the role of transposable elements in human genetic disease with particular attention to achondroplasia and the fragile X syndromeS F Hoegerman, J M RaryObstetrics and Gynecology|January 1, 1978
The fallability of X-chromatin as a screening test for anomalies of the X chromosomeJ M Rary, D Cummings, H W JonesThe Journal of Heredity|November 1, 1983
Double balanced chromosomal translocation carrier (6;8), (13;14)--a case reportR G Hansen, R L Anderson, J M RaryThe Journal of Heredity|January 1, 1979
Assignment of the H-Y antigen gene to the short arm of chromosome YJ M Rary, D K Cummings, H W Jones, et al.Clinical Genetics|January 1, 1977
Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12)P N Howard-Peebles, K M Yarbrough, G R Stoddard, et al.Pageof 12