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Obstetrics and Gynecology|October 1, 1995
DNA-based prenatal determination of the RhEe genotypeW C Spence, P Potter, A Maddalena, et al.Obstetrics and Gynecology|February 1, 1995
Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic diseaseW C Spence, A Maddalena, D B Demers, et al.The Journal of Reproductive Medicine|June 1, 1997
Prenatal determination of genotypes Kell and Cellano in at-risk pregnanciesW C Spence, A Maddalena, D B Demers, et al.The Journal of Reproductive Medicine|May 1, 1992
Molecular diagnosis of genetic diseaseA Maddalena, D P Bick, J D SchulmanAmerican Journal of Medical Genetics|July 12, 1996
Molecular fragile X screening in normal populationsW C Spence, S H Black, L Fallon, et al.American Journal of Medical Genetics|August 9, 1996
A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in bloodA Maddalena, K N Yadvish, W C Spence, et al.American Journal of Medical Genetics|July 15, 1994
Prenatal diagnosis in known fragile X carriersA Maddalena, B D Hicks, W C Spence, et al.American Journal of Medical Genetics|July 15, 1994
Improved sizing of fragile X CCG repeats by nested polymerase chain reactionG Levinson, A Maddalena, F T Palmer, et al.Current Protocols in Human Genetics|April 23, 2008
Molecular analysis of paternityA C Sozer, C M Kelly, D B DemersThe Journal of Reproductive Medicine|June 4, 1998
Screening semen donors for hereditary diseases. The Fairfax cryobank experienceD Bick, E F Fugger, S H Pool, et al.Pageof 16