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American Journal of Medical Genetics|January 10, 1997
Carrier testing in the fragile X syndrome: attitudes and opinions of obligate carriersA McConkie-Rosell, G A Spiridigliozzi, T Iafolla, et al.
American Journal of Human Genetics|October 1, 1992
Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophyL S Schwartz, J Tarleton, B Popovich, et al.
Biology of Reproduction|July 23, 1998
Keratinocyte growth factor expression by the bovine corpus luteumU Salli, F F Bartol, A A Wiley, et al.
American Journal of Medical Genetics|August 9, 1996
Rater reliability of fragile X mutation size estimates: a multilaboratory analysisG S Fisch, N Carpenter, A Maddalena, et al.
Biology of Reproduction|April 18, 1998
Ovary-independent estrogen receptor expression in neonatal porcine endometriumB J Tarleton, A A Wiley, T E Spencer, et al.
American Journal of Medical Genetics|August 9, 1996
A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 geneA M Lachiewicz, G A Spiridigliozzi, A McConkie-Rosell, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
American Journal of Medical Genetics|August 9, 1996
Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: a prospective multicenter analysisG S Fisch, R Simensen, J Tarleton, et al.
American Journal of Medical Genetics|January 2, 1995
Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion regionR C Michaelis, S A Skinner, B A Lethco, et al.
American Journal of Human Genetics|August 1, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 casesF Rousseau, D Heitz, J Tarleton, et al.
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