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Results: 1-16 |
Results: 16
EFFICIENCY OF MICROSORT FLOW-CYTOMETRY FOR PRODUCING SPERM POPULATIONS ENRICHED IN X-CHROMOSOME OR Y-CHROMOSOME HAPLOTYPES - A BLIND TRIAL ASSESSED BY DOUBLE AND TRIPLE COLOR FLUORESCENT IN-SITU HYBRIDIZATION
Authors: VIDAL F FUGGER EF BLANCO J KEYVANFAR K CATALA V NORTON M HAZELRIGG WB BLACK SH LEVINSON G EGOZCUE J SCHULMAN JD
Citation: F. Vidal et al., EFFICIENCY OF MICROSORT FLOW-CYTOMETRY FOR PRODUCING SPERM POPULATIONS ENRICHED IN X-CHROMOSOME OR Y-CHROMOSOME HAPLOTYPES - A BLIND TRIAL ASSESSED BY DOUBLE AND TRIPLE COLOR FLUORESCENT IN-SITU HYBRIDIZATION, Human reproduction, 13(2), 1998, pp. 308-312
100 REFERRALS TO AN EATING DISORDERS SERVICE - PROGRESS AND SERVICE CONSUMPTION OVER A 2-4-YEAR PERIOD
Authors: BUTTON EJ MARSHALL P SHINKWIN R BLACK SH PALMER RL
Citation: Ej. Button et al., 100 REFERRALS TO AN EATING DISORDERS SERVICE - PROGRESS AND SERVICE CONSUMPTION OVER A 2-4-YEAR PERIOD, European eating disorders review, 5(1), 1997, pp. 47-63
PREIMPLANTATION GENETIC DIAGNOSIS IN MARFAN-SYNDROME
Authors: KILPATRICK MW HARTON GL PHYLACTOU LA LEVINSON G FUGGER EF SCHULMAN JD BLACK SH TSIPOURAS P
Citation: Mw. Kilpatrick et al., PREIMPLANTATION GENETIC DIAGNOSIS IN MARFAN-SYNDROME, Fetal diagnosis and therapy, 11(6), 1996, pp. 402-406
PRENATAL-DIAGNOSIS OF UNIPARENTAL DISOMY-15 FOLLOWING TRISOMY-15 MOSAICISM
Authors: CHRISTIAN SL SMITH ACM MACHA M BLACK SH ELDER FFB JOHNSON JMP RESTA RG SURTI U SUSLAK L VERP MS LEDBETTER DH
Citation: Sl. Christian et al., PRENATAL-DIAGNOSIS OF UNIPARENTAL DISOMY-15 FOLLOWING TRISOMY-15 MOSAICISM, Prenatal diagnosis, 16(4), 1996, pp. 323-332
MOLECULAR FRAGILE-X SCREENING IN NORMAL-POPULATIONS
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
PREIMPLANTATION GENETIC TESTING FOR HUNTINGTON DISEASE AND CERTAIN OTHER DOMINANTLY INHERITED DISORDERS
Authors: SCHULMAN JD BLACK SH HANDYSIDE A NANCE WE
Citation: Jd. Schulman et al., PREIMPLANTATION GENETIC TESTING FOR HUNTINGTON DISEASE AND CERTAIN OTHER DOMINANTLY INHERITED DISORDERS, Clinical genetics, 49(2), 1996, pp. 57-58
NUCLEATED ERYTHROCYTES IN MATERNAL BLOOD - QUANTITY AND QUALITY OF FETAL CELLS IN ENRICHED POPULATIONS
Authors: READING JP HUFFMAN JL WU JC PALMER FT HARTON GL SISSON ME KEYVANFAR K GRESINGER TH COCHRANE WJ FALLON LA MENAPACEDREW GF CUMMINGS EA JONES SL BLACK SH SCHULMAN JD LEVINSON G
Citation: Jp. Reading et al., NUCLEATED ERYTHROCYTES IN MATERNAL BLOOD - QUANTITY AND QUALITY OF FETAL CELLS IN ENRICHED POPULATIONS, Human reproduction, 10(9), 1995, pp. 2510-2515
DNA-BASED X-ENRICHED SPERM SEPARATION AS AN ADJUNCT TO PREIMPLANTATION GENETIC TESTING FOR THE PREVENTION OF X-LINKED DISEASE
Authors: LEVINSON G KEYVANFAR K WU JC FUGGER EF FIELDS RA HARTON GL PALMER FT SISSON ME STARR KM DENNISONLAGOS L CALVO L SHERINS RJ BICK D SCHULMAN JD BLACK SH
Citation: G. Levinson et al., DNA-BASED X-ENRICHED SPERM SEPARATION AS AN ADJUNCT TO PREIMPLANTATION GENETIC TESTING FOR THE PREVENTION OF X-LINKED DISEASE, Human reproduction, 10(4), 1995, pp. 979-982
PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX)
Authors: BLACK SH LEVINSON G HARTON GL PALMER FT SISSON ME SCHOENER C NANCE C FUGGER EF FIELDS RA
Citation: Sh. Black et al., PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX), American journal of human genetics, 57(4), 1995, pp. 153-153
PRENATAL-DIAGNOSIS OF SJOGREN-LARSSON SYNDROME USING ENZYMATIC METHODS
Authors: RIZZO WB CRAFT DA KELSON TL BONNEFONT JP SAUDUBRAY JM SCHULMAN JD BLACK SH TABSH K DIROCCO M GARDNER RJM
Citation: Wb. Rizzo et al., PRENATAL-DIAGNOSIS OF SJOGREN-LARSSON SYNDROME USING ENZYMATIC METHODS, Prenatal diagnosis, 14(7), 1994, pp. 577-581
FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE
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
MENTAL-RETARDATION AND ULLRICH-TURNER SYNDROME IN CASES WITH 45,X 46,X,+MAR - ADDITIONAL SUPPORT FOR THE LOSS OF THE X-INACTIVATION CENTER HYPOTHESIS/
Authors: COLE H HUANG B SALBERT BA BROWN J HOWARDPEEBLES PN BLACK SH DORFMANN A FEBLES OR STEVENS CA JACKSONCOOK C
Citation: H. Cole et al., MENTAL-RETARDATION AND ULLRICH-TURNER SYNDROME IN CASES WITH 45,X 46,X,+MAR - ADDITIONAL SUPPORT FOR THE LOSS OF THE X-INACTIVATION CENTER HYPOTHESIS/, American journal of medical genetics, 52(2), 1994, pp. 136-145
IMPROVED SIZING OF FRAGILE-X CCG REPEATS BY NESTED POLYMERASE CHAIN-REACTION
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
PREGNANCY SCREENING FOR CYSTIC-FIBROSIS
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
PRENATAL-DIAGNOSIS OF SJOGREN-LARSSON SYNDROME IN THE 1ST AND 2ND TRIMESTER USING ENZYMATIC METHODS
Authors: RIZZO WB CRAFT DA KELSON L BONNEFONT JP SAUDUBRAY JM SCHULMAN JD BLACK SH TABSH K DIROCCO M
Citation: Wb. Rizzo et al., PRENATAL-DIAGNOSIS OF SJOGREN-LARSSON SYNDROME IN THE 1ST AND 2ND TRIMESTER USING ENZYMATIC METHODS, American journal of human genetics, 53(3), 1993, pp. 89-89
TRIPLICATION 15Q11-13 IN 2 UNRELATED PATIENTS WITH HYPOTONIA, COGNITIVE DELAYS AND VISUAL IMPAIRMENT
Authors: HOLOWINSKY S BLACK SH HOWARDPEEBLES PN MUTIRANGURA A CHRISTIAN S LEDBETTER DH REYNOLDS J
Citation: S. Holowinsky et al., TRIPLICATION 15Q11-13 IN 2 UNRELATED PATIENTS WITH HYPOTONIA, COGNITIVE DELAYS AND VISUAL IMPAIRMENT, American journal of human genetics, 53(3), 1993, pp. 125-125
Risultati: 1-16 |