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Clinical Chemistry|November 1, 1991
Rapid diagnosis of familial defective apolipoprotein B-100 by Amplification Refractory Mutation SystemP R Wenham, C R Newton, R S Houlston, et al.The British Journal of Radiology|March 1, 1996
Case report: MRI appearances of left sided Morgagni hernia containing liverD A Collie, C M Turnbull, T R Shaw, et al.Human Genetics|May 1, 1986
The effect of caffeine on fragile X expressionM A Abruzzo, D Pettay, M Mayer, et al.Genetic Epidemiology|January 1, 1984
Complete hydatidiform mole in Hawaii: an epidemiological studyJ Matsuura, D Chiu, P A Jacobs, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnanciesR S James, K Ellis, D Pettay, et al.Journal of the American Chemical Society|August 23, 2001
Use of WO(4)(2-) on layered double hydroxides for mild oxidative bromination and bromide-assisted epoxidation with H(2)O(2)B F Sels, D E De Vos, P A JacobsAnnals of Human Genetics|July 1, 1988
Maternal age in trisomyN E Morton, P A Jacobs, T Hassold, et al.Journal of Epidemiology and Community Health|December 1, 1985
Causes of death in X chromatin positive males (Klinefelter's syndrome)W H Price, J F Clayton, J Wilson, et al.Journal of Epidemiology and Community Health|June 1, 1986
Mortality ratios, life expectancy, and causes of death in patients with Turner's syndromeW H Price, J F Clayton, S Collyer, et al.American Journal of Human Genetics|July 1, 1981
Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21P A Jacobs, P A Hunt, M Mayer, et al.Pageof 17