Authors:
BICK D
FUGGER EE
POOL SH
HAZELRIGG WB
YADVISH KN
SPENCE WC
MADDALENA A
HOWARDPEEBLES PN
SCHULMAN JD
Citation: D. Bick et al., SCREENING SEMEN DONORS FOR HEREDITARY-DISEASES - THE FAIRFAX CRYOBANKEXPERIENCE, Journal of reproductive medicine, 43(5), 1998, pp. 423-428
Citation: Wc. Spence et al., PRENATAL DETERMINATION OF GENOTYPES KELL AND CELLANO IN AT-RISK PREGNANCIES, Journal of reproductive medicine, 42(6), 1997, pp. 353-357
Authors:
MADDALENA A
YADVISH KN
SPENCE WC
HOWARDPEEBLES PN
Citation: A. Maddalena et al., A FRAGILE-X MOSAIC MALE WITH A CRYPTIC FULL MUTATION DETECTED IN EPITHELIUM BUT NOT IN BLOOD, American journal of medical genetics, 64(2), 1996, pp. 309-312
Authors:
SPENCE WC
MADDALENA A
HOWARDPEEBLES PN
BICK DP
Citation: Wc. Spence et al., CONTRIBUTION OF THE MOLECULAR-GENETICS LABORATORY TO THE EVALUATION OF THE PERSISTENTLY HYPOTONIC INFANT, Pediatric research, 39(4), 1996, pp. 872-872
Citation: Wc. Spence et al., MOLECULAR ANALYSIS OF THE RHD GENOTYPE IN FETUSES AT RISK FOR RHD HEMOLYTIC-DISEASE, Obstetrics and gynecology, 85(2), 1995, pp. 296-298
Citation: A. Maddalena et al., PRENATAL DETECTION OF RHD, RHC, RHE, AND KELL GENOTYPES FOR MANAGEMENT OF PREGNANCIES AT RISK FOR HEMOLYTIC-DISEASE OF THE NEWBORN, American journal of human genetics, 57(4), 1995, pp. 256-256
Citation: Wc. Spence et al., MOLECULAR CONFIRMATION OF ALPHA(1)-ANTITRYPSIN GENOTYPES IN NEWBORN DRIED BLOOD SPECIMENS, Biochemical medicine and metabolic biology, 50(2), 1993, pp. 233-240
Authors:
SPENCE WC
PAULUSTHOMAS J
ORENSTEIN DM
NAYLOR EW
Citation: Wc. Spence et al., NEONATAL SCREENING FOR CYSTIC-FIBROSIS - ADDITION OF MOLECULAR DIAGNOSTICS TO INCREASE SPECIFICITY, Biochemical medicine and metabolic biology, 49(2), 1993, pp. 200-211
Authors:
PAULUSTHOMAS J
SPENCE WC
MIKLOS J
LANTSY A
Citation: J. Paulusthomas et al., RAPID IDENTIFICATION OF NEWBORNS WITH ALPHA-1-ANTITRYPSIN DEFICIENCY USING A FLUOROMETRIC SCREENING AND MULTIPLEX PCR ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 1500-1500