Multilocus analysis of the fragile X syndromeW. Ted Brown, Nancy J. Carpenter, Kim Summers et al.|Human Genetics|1988Cited by 59
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
Molecular approaches to carrier detection and prenatal diagnosis of the fragile x syndromePatricia D. Murphy, W. Roy Breg, M. Watson et al.|Unknown|1988Cited by 5
DNA‐based genetic testing in fifty fragile X familiesPatricia D. Murphy, W. Roy Breg, M. Watson et al.|American Journal of Medical Genetics|1991Cited by 2
Molecular analysis of a case with a non fluorescent y chromosome 45 x 46 xy non fluorescentPatricia D. Murphy, W. Roy Breg, M. Watson et al.|Unknown|1985Cited by 0