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American 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 Rary
Obstetrics 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 Jones
The Journal of Heredity|January 1, 1975
A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasiaJ M Rary, M A Bender, T E Kelly
Mutation Research|June 1, 1985
G0 chromosomal radiosensitivity in ataxia telangiectasia lymphocytesM A Bender, J M Rary, R P Kale
Mutation Research|October 1, 1985
G2 chromosomal radiosensitivity in ataxia telangiectasia lymphocytesM A Bender, J M Rary, R P Kale
The 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 Rary
Mutation Research|November 1, 1979
G2 chromosomal radiosensitivity in Fanconi's anemiaS B Bigelow, J M Rary, M A Bender
The 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.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1977
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variantsL M Kunkel, K D Smith, S H Boyer, et al.
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