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Results: 1-14 |
Results: 14

Authors: LAYMAN LC COHEN DP JIN M XIE J LI Z REINDOLLAR RH BOLBOLAN S BICK DP SHERINS RR DUCK LW MUSGROVE LC SELLERS JC NEILL JD
Citation: Lc. Layman et al., MUTATIONS IN GONADOTROPIN-RELEASING-HORMONE RECEPTOR GENE CAUSE HYPOGONADOTROPIC HYPOGONADISM, Nature genetics, 18(1), 1998, pp. 14-15

Authors: SPENCE WC MADDALENA A DEMERS DB BICK DP
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: BICK DP STANLEY WS STERN HJ BERKOVITZ GD MEYERS CM KELLEY RI
Citation: Dp. Bick et al., PRENATAL-DIAGNOSIS OF SMITH-LEMLI-OPITZ-SYNDROME (SLO) IN A SEX-REVERSED FETUS, American journal of human genetics, 61(4), 1997, pp. 838-838

Authors: SPENCE WC BLACK SH FALLON L MADDALENA A CUMMINGS E MENAPACEDREW G BICK DP LEVINSON G SCHULMAN JD HOWARDPEEBLES PN
Citation: Wc. Spence et al., MOLECULAR FRAGILE-X SCREENING IN NORMAL-POPULATIONS, American journal of medical genetics, 64(1), 1996, pp. 181-183

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

Authors: SPENCE WC POTTER P MADDALENA A DEMERS DB BICK DP
Citation: Wc. Spence et al., DNA-BASED PRENATAL DETERMINATION OF THE RHEE GENOTYPE, Obstetrics and gynecology, 86(4), 1995, pp. 670-672

Authors: SPENCE WC MADDALENA A DEMERS DB BICK DP
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

Authors: MADDALENA A SPENCE WC DEMERS DB BICK DP
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

Authors: HOWARDPEEBLES PN MADDALENA A SPENCE WC LEVINSON G FALLON L BICK DP BLACK SH SCHULMAN JD
Citation: Pn. Howardpeebles et al., FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE, American journal of medical genetics, 53(4), 1994, pp. 382-382

Authors: LEVINSON G MADDALENA A PALMER FT HARTON GL BICK DP HOWARDPEEBLES PN BLACK SH SCHULMAN JD
Citation: G. Levinson et al., IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION, American journal of medical genetics, 51(4), 1994, pp. 527-534

Authors: SPENCE WC MADDALENA A DEMERS DB BICK DP
Citation: Wc. Spence et al., MOLECULAR ANALYSIS OF THE RH LOCUS IN A PERSON WITH THE D-U PHENOTYPE, Transfusion, 34(8), 1994, pp. 741-742

Authors: BICK DP BALLABIO A
Citation: Dp. Bick et A. Ballabio, BRINGING KALLMANN SYNDROME INTO FOCUS, American journal of neuroradiology, 14(4), 1993, pp. 852-854

Authors: BLACK SH BICK DP MADDALENA A SCHULMAN JD JONES SL FALLON L CUMMINGS E MENAPACEDREW G
Citation: Sh. Black et al., PREGNANCY SCREENING FOR CYSTIC-FIBROSIS, Lancet, 342(8879), 1993, pp. 1112-1113

Authors: STETKA DG BICK DP MECK JM BATY EB SCHULMAN JD
Citation: Dg. Stetka et al., 2 CASES OF MOSAIC VARIEGATED ANEUPLOIDY WITH MICROCEPHALY - A MUTATION THAT RESULTS IN MITOTIC NONDISJUNCTION, American journal of human genetics, 53(3), 1993, pp. 604-604
Risultati: 1-14 |