Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: Amniotic fluid, chorionic villi, fetal blood and molecular methodsLawrence R. Shapiro, W. Roy Breg, Patrick L. Wilmot et al.|American Journal of Medical Genetics|1988Cited by 22
Prenatal diagnosis of the fragile X syndrome: Possible end of the experimental phase for amniotic fluidLawrence R. Shapiro, Patricia D. Murphy, Patrick L. Wilmot|American Journal of Medical Genetics|1991Cited by 8
Molecular approaches to carrier detection and prenatal diagnosis of the fragile x syndromePatricia D. Murphy, W. Roy Breg, Lawrence R. Shapiro et al.|Unknown|1988Cited by 5
Prenatal diagnosis of fragile X syndrome: Results from parallel molecular and cytogenetic studiesPatricia D. Murphy, Lawrence R. Shapiro, Patrick L. Wilmot|American Journal of Medical Genetics|1992Cited by 3
DNA‐based genetic testing in fifty fragile X familiesPatricia D. Murphy, W. Roy Breg, Patrick L. Wilmot et al.|American Journal of Medical Genetics|1991Cited by 2