WilliamCraigSpenceMD

PubMed

• Identification of a 55-bp deletion in the glucocerebrosidase gene in Gaucher disease: phenotypic presentation and implications for mutation detection assays.
  Mao, R., O'Brien, J.F., Rao, S., Schmitt, E., Roa, B., Feldman, G.L., Spence, W.C., Snow, K.> ;Mol Genet Metab. 2001 Mar
• Screening semen donors for hereditary diseases. The Fairfax cryobank experience.
  Bick, D., Fugger, E.F., Pool, S.H., Hazelrigg, W.B., Yadvish, K.N., Spence, W.C., Maddalena, A., Howard-Peebles, P.N., Schulman, J.D.> ;J Reprod Med. 1998 May
• Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies.
  Spence, W.C., Maddalena, A., Demers, D.B., Bick, D.P.> ;J Reprod Med. 1997 Jun
• A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood.
  Maddalena, A., Yadvish, K.N., Spence, W.C., Howard-Peebles, P.N.> ;Am J Med Genet. 1996 Aug 9
• Molecular fragile X screening in normal populations.
  Spence, W.C., Black, S.H., Fallon, L., Maddalena, A., Cummings, E., Menapace-Drew, G., Bick, D.P., Levinson, G., Schulman, J.D., Howard-Peebles, P.N.> ;Am J Med Genet. 1996 Jul 12
• DNA-based prenatal determination of the RhEe genotype.
  Spence, W.C., Potter, P., Maddalena, A., Demers, D.B., Bick, D.P.> ;Obstet Gynecol. 1995 Oct
• Recent advances in reproductive genetic technologies.
  Levinson, G., Coulam, C.B., Spence, W.C., Sherins, R.J., Schulman, J.D.> ;Biotechnology (N Y). 1995 Sep
• Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease.
  Spence, W.C., Maddalena, A., Demers, D.B., Bick, D.P.> ;Obstet Gynecol. 1995 Feb
• Neonatal screening for cystic fibrosis: addition of molecular diagnostics to increase specificity.
  Spence, W. C., Paulus-Thomas, J., Orenstein, D. M., Naylor, E. W.> ;Biochem Med Metab Biol. 1993 Apr
• Molecular confirmation of alpha 1-antitrypsin genotypes in newborn dried blood specimens.
  Spence, W. C., Morris, J. E., Pass, K., Murphy, P. D.> ;Biochem Med Metab Biol. 1993 Oct
• Molecular analysis of the Rh locus in a person with the Du phenotype.
  Spence, W. C., Maddalena, A., Demers, D. B., Bick, D. P.> ;Transfusion. 1994 Aug
• Fragile X screening: what is the real issue?
  Howard-Peebles, P. N., Maddalena, A., Spence, W. C., Levinson, G., Fallon, L., Bick, D. P., Black, S. H., Schulman, J. D.> ;Am J Med Genet. 1994 Dec 1
• Prenatal diagnosis in known fragile X carriers.
  Maddalena, A., Hicks, B. D., Spence, W. C., Levinson, G., Howard-Peebles, P. N.> ;Am J Med Genet. 1994 Jul 15
• Join now to see all