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Human Molecular Genetics|March 1, 1996
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndromeE E Eichler, J N Macpherson, A Murray, et al.European Journal of Human Genetics : EJHG|January 1, 1994
A systematic search for uniparental disomy in carriers of chromosome translocationsR S James, I K Temple, C Patch, et al.Journal of Medical Genetics|June 1, 1993
Population studies of the fragile X: a molecular approachP A Jacobs, H Bullman, J Macpherson, et al.Annals of Human Genetics|May 1, 1988
Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probesP A Jacobs, T J Hassold, E Whittington, et al.Annals of Human Genetics|January 1, 1990
A centromere map of the X chromosome from trisomies of maternal originN E Morton, B J Keats, P A Jacobs, et al.American Journal of Human Genetics|July 1, 1982
Expression of the marker (X) (q28) in lymphoblastoid cell linesP A Jacobs, P A Hunt, M Mayer, et al.Cytogenetics and Cell Genetics|January 1, 1986
Cytogenetic analysis of lymphoblastoid cell linesM A Abruzzo, P A Hunt, M Mayer, et al.American Journal of Human Genetics|April 1, 1986
A comparison of fragile X expression in lymphocyte and lymphoblastoid culturesM A Abruzzo, P A Hunt, M Mayer, et al.American Journal of Human Genetics|April 1, 1990
The parental origin of the extra X chromosome in 47,XXX femalesK M May, P A Jacobs, M Lee, et al.Annals of Human Genetics|July 1, 1978
The origin of human triploidsP A Jacobs, R R Angell, I M Buchanan, et al.Pageof 17