-
1
-
-
0033656961
-
Chorion villus sampling versus amniocentesis for prenatal diagnosis (Cochrane Review)
-
Update Software: Oxford
-
Alfirevic Z, Gosden C, Neilson JP. 1998. Chorion villus sampling versus amniocentesis for prenatal diagnosis (Cochrane Review). In The Cochrane Library, Issue 3. Update Software: Oxford.
-
(1998)
The Cochrane Library
, Issue.3
-
-
Alfirevic, Z.1
Gosden, C.2
Neilson, J.P.3
-
2
-
-
0027293541
-
Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals
-
Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. 1993. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood 82: 651-655.
-
(1993)
Blood
, vol.82
, pp. 651-655
-
-
Arce, M.A.1
Thompson, E.S.2
Wagner, S.3
Coyne, K.E.4
Ferdman, B.A.5
Lublin, D.M.6
-
3
-
-
0029949995
-
Kell typing by allele-specific PCR (ASP)
-
Avent ND, Martin PG. 1996. Kell typing by allele-specific PCR (ASP). Br J Haemat 93: 728-730.
-
(1996)
Br J Haemat
, vol.93
, pp. 728-730
-
-
Avent, N.D.1
Martin, P.G.2
-
4
-
-
0342531273
-
Molecular basis of the DVI variant phenotype: Evidence that a RHD deletion event does not generate all cDVIE haplotypes
-
3us P1C7, 1996 (abstract)
-
Avent ND, Jones JW, Liu W, Scott ML, Voak D, Pisacka M, Watt J, Fletcher A. 1996. Molecular basis of the DVI variant phenotype: evidence that a RHD deletion event does not generate all cDVIE haplotypes. Tranf Clin et Biol 3: 3us P1C7, 1996 (abstract).
-
(1996)
Tranf Clin et Biol
, vol.3
-
-
Avent, N.D.1
Jones, J.W.2
Liu, W.3
Scott, M.L.4
Voak, D.5
Pisacka, M.6
Watt, J.7
Fletcher, A.8
-
5
-
-
0030057292
-
Characterization of the hybrid RHD gene leading to the partial D category IIIC phenotype
-
Beckers EAM, Faas BHW, Ligthart P, Simsek S, Overbeeke MAM, von dem Borne AEGKR, van Rhenen DY, van der School CE. 1996a. Characterization of the hybrid RHD gene leading to the partial D category IIIC phenotype. Transfusion 36: 567-574.
-
(1996)
Transfusion
, vol.36
, pp. 567-574
-
-
Beckers, E.A.M.1
Faas, B.H.W.2
Ligthart, P.3
Simsek, S.4
Overbeeke, M.A.M.5
Von Dem Borne, A.E.G.K.R.6
Van Rhenen, D.Y.7
Van Der School, C.E.8
-
6
-
-
0029938326
-
The genetic basis of a new partial D antigen: D DBT
-
Beckers EAM, Faas BHW, Overbeeke MAM, van Rhenen DY, Wallace M, von dem Borne AEGKR, van der School CE, 1996b. The genetic basis of a new partial D antigen: D DBT. Br J Haemat 93: 720-727.
-
(1996)
Br J Haemat
, vol.93
, pp. 720-727
-
-
Beckers, E.A.M.1
Faas, B.H.W.2
Overbeeke, M.A.M.3
Van Rhenen, D.Y.4
Wallace, M.5
Von Dem Borne, A.E.G.K.R.6
Van Der School, C.E.7
-
7
-
-
0029670163
-
The R0Har phenotype resulls from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene
-
Beckers EAM, Faas BHW, Von dem Borne AEGKr, Overbeeke MAM, Van Rhenen DJ, Van der Schoot CE. 1996c. The R0Har phenotype resulls from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene. Br J Haemat 92: 751-757.
-
(1996)
Br J Haemat
, vol.92
, pp. 751-757
-
-
Beckers, E.A.M.1
Faas, B.H.W.2
Von Dem Borne, A.E.G.Kr.3
Overbeeke, M.A.M.4
Van Rhenen, D.J.5
Van Der Schoot, C.E.6
-
8
-
-
0027216648
-
Prenatal determination of fetal RhD type by DNA amplification
-
Bennett PR, Le Van Kim C, Colin Y, Warwick RM, Chérif-Zahar B, Fisk NM, Cartron J-P. 1993. Prenatal determination of fetal RhD type by DNA amplification. N Engl J Med 329: 607-610.
-
(1993)
N Engl J Med
, vol.329
, pp. 607-610
-
-
Bennett, P.R.1
Le Van Kim, C.2
Colin, Y.3
Warwick, R.M.4
Chérif-Zahar, B.5
Fisk, N.M.6
Cartron, J.-P.7
-
9
-
-
0027993037
-
Serotype switching in a partially deleted RhD gene
-
Blunt T, Daniels G, Carritt B. 1994. Serotype switching in a partially deleted RhD gene. Vox Sang 67: 397-401.
-
(1994)
Vox Sang
, vol.67
, pp. 397-401
-
-
Blunt, T.1
Daniels, G.2
Carritt, B.3
-
10
-
-
0030853605
-
Differences between RhD-negative Africans and RhD-negative Europeans
-
Daniels G, Green C, Smart E. 1997. Differences between RhD-negative Africans and RhD-negative Europeans. Lancet 350: 862.
-
(1997)
Lancet
, vol.350
, pp. 862
-
-
Daniels, G.1
Green, C.2
Smart, E.3
-
11
-
-
0030222022
-
Determination of fetal RhD status from uncultured amniocytes
-
Dildy GA, Jackson GM, Ward K. 1996. Determination of fetal RhD status from uncultured amniocytes. Obstet Gynecol 88: 207-210.
-
(1996)
Obstet Gynecol
, vol.88
, pp. 207-210
-
-
Dildy, G.A.1
Jackson, G.M.2
Ward, K.3
-
12
-
-
0027787872
-
Complications of ultrasound-guided percutaneous umbilical blood sampling: Analysis of a series of 341 cases and review of the literature
-
Duchatel F, Aury JF, Mennesson B. 1993. Complications of ultrasound-guided percutaneous umbilical blood sampling: analysis of a series of 341 cases and review of the literature. Eur J Obstet Gynecol Reprod Biol 52: 95-104.
-
(1993)
Eur J Obstet Gynecol Reprod Biol
, vol.52
, pp. 95-104
-
-
Duchatel, F.1
Aury, J.F.2
Mennesson, B.3
-
13
-
-
0028939296
-
Rh E/e-genotyping by allele-specific primer amplification (ASPA)
-
Faas BHW, Simsek S, Bleeker PMM, Overbeeke MAM, Cuỳpers TH, von dem Borne AEGKR, van der School CE. 1995. Rh E/e-genotyping by allele-specific primer amplification (ASPA). Blood 85: 829-832.
-
(1995)
Blood
, vol.85
, pp. 829-832
-
-
Faas, B.H.W.1
Simsek, S.2
Bleeker, P.M.M.3
Overbeeke, M.A.M.4
Cuỳpers, T.H.5
Von Dem Borne, A.E.G.K.R.6
Van Der School, C.E.7
-
14
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas BHW, Beckers EAM, Wildoer P, Ligthart PC, Overbeeke MAM, Zondervan HA, von dem Borne AEGKR, van der Schoot CE. 1997. Molecular background of VS and weak C expression in blacks. Transfusion 37: 38-44.
-
(1997)
Transfusion
, vol.37
, pp. 38-44
-
-
Faas, B.H.W.1
Beckers, E.A.M.2
Wildoer, P.3
Ligthart, P.C.4
Overbeeke, M.A.M.5
Zondervan, H.A.6
Von Dem Borne, A.E.G.K.R.7
Van Der Schoot, C.E.8
-
15
-
-
0028070609
-
Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villi
-
Fisk NM, Bennett P, Warwick RM, Letsky EA, Welch R. 1994. Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villi. Am J Obstet Gynecol 171: 50-54.
-
(1994)
Am J Obstet Gynecol
, vol.171
, pp. 50-54
-
-
Fisk, N.M.1
Bennett, P.2
Warwick, R.M.3
Letsky, E.A.4
Welch, R.5
-
17
-
-
0025899530
-
Amniocentesis or chorionic villus sampling for prenatal genetic testing: A decision analysis
-
Heckerling PS, Verp MS. 1991. Amniocentesis or chorionic villus sampling for prenatal genetic testing: a decision analysis. J Clin Epidemiol 44: 657-670.
-
(1991)
J Clin Epidemiol
, vol.44
, pp. 657-670
-
-
Heckerling, P.S.1
Verp, M.S.2
-
18
-
-
0030017853
-
Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers
-
Hessner MJ, McFarland JG, Endean DJ. 1996. Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers. Transfusion 36: 495-499.
-
(1996)
Transfusion
, vol.36
, pp. 495-499
-
-
Hessner, M.J.1
McFarland, J.G.2
Endean, D.J.3
-
19
-
-
0028241841
-
Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r′r′) phenotypes
-
Hyland CA, Wolter LC, Saul A. 1994. Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r′r′) phenotypes. Blood 84: 321-324.
-
(1994)
Blood
, vol.84
, pp. 321-324
-
-
Hyland, C.A.1
Wolter, L.C.2
Saul, A.3
-
20
-
-
0028936247
-
Molecular basis of the Kell (K1) phenotype
-
Lee S, Wu X, Reid M, Zelinski T, Redman C. 1995. Molecular basis of the Kell (K1) phenotype. Blood 85: 912-916.
-
(1995)
Blood
, vol.85
, pp. 912-916
-
-
Lee, S.1
Wu, X.2
Reid, M.3
Zelinski, T.4
Redman, C.5
-
21
-
-
0028070411
-
PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease
-
Le Van Kim C, Mouro I, Brossard Y, Chavinie J, Cartron JP, Colin Y. 1994. PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease. Br J Haemat 8864: 193-195.
-
(1994)
Br J Haemat
, vol.8864
, pp. 193-195
-
-
Le Van Kim, C.1
Mouro, I.2
Brossard, Y.3
Chavinie, J.4
Cartron, J.P.5
Colin, Y.6
-
22
-
-
0028784313
-
Accuracy of prenatal determination of RhD type status by polymerase chain reaction with amniotic cells
-
Lighten AD, Overton TG, Sepulveda W, Warwick RM, Fisk NM, Bennett PR. 1995. Accuracy of prenatal determination of RhD type status by polymerase chain reaction with amniotic cells. Am J Obstet Gynecol 4: 1182-1185.
-
(1995)
Am J Obstet Gynecol
, vol.4
, pp. 1182-1185
-
-
Lighten, A.D.1
Overton, T.G.2
Sepulveda, W.3
Warwick, R.M.4
Fisk, N.M.5
Bennett, P.R.6
-
23
-
-
0030760264
-
Evidence that the RHD(VI) deletion genotype does not exist
-
Maaskant-van Wijk PA, Beckers EAM, van Rhenen DJ, Mouro I, Colin Y, Cartron J-P, Faas BHW, van der School CE, Apoil PA, Blancher A, von dem Borne AEGKR. 1997. Evidence that the RHD(VI) deletion genotype does not exist. Blood 99: 1709-1711.
-
(1997)
Blood
, vol.99
, pp. 1709-1711
-
-
Maaskant-Van Wijk, P.A.1
Beckers, E.A.M.2
Van Rhenen, D.J.3
Mouro, I.4
Colin, Y.5
Cartron, J.-P.6
Faas, B.H.W.7
Van Der School, C.E.8
Apoil, P.A.9
Blancher, A.10
Von Dem Borne, A.E.G.K.R.11
-
24
-
-
0031768108
-
Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons
-
Maaskant-van Wijk PA, Faas BHW, de Ruijter JA, Overbeeke MAM, von dem Borne AEGKr, van Rhenen DJ, van der School CE. 1998. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons. Transfusion 38: 1015-1021.
-
(1998)
Transfusion
, vol.38
, pp. 1015-1021
-
-
Maaskant-Van Wijk, P.A.1
Faas, B.H.W.2
De Ruijter, J.A.3
Overbeeke, M.A.M.4
Von Dem Borne, A.E.G.K.R.5
Van Rhenen, D.J.6
Van Der School, C.E.7
-
25
-
-
0027958599
-
Rearrangements of the blood group RhD gene associated with the D-VI category phenotype
-
Mouro I, Le Van Kim C, Rouillac C, van Rhenen DY, La Pennec PY, Bailly P, Cartron J-P, Colin Y. 1994. Rearrangements of the blood group RhD gene associated with the D-VI category phenotype. Blood 83: 1129-1135.
-
(1994)
Blood
, vol.83
, pp. 1129-1135
-
-
Mouro, I.1
Le Van Kim, C.2
Rouillac, C.3
Van Rhenen, D.Y.4
La Pennec, P.Y.5
Bailly, P.6
Cartron, J.-P.7
Colin, Y.8
-
26
-
-
0030158309
-
Development of a PCR-based diagnostic assay for the determination of the KEL genotype in donor blood samples
-
Murphy MT, Fraser RH, Goddard JP. 1996. Development of a PCR-based diagnostic assay for the determination of the KEL genotype in donor blood samples. Transfus Med 6: 133-137.
-
(1996)
Transfus Med
, vol.6
, pp. 133-137
-
-
Murphy, M.T.1
Fraser, R.H.2
Goddard, J.P.3
-
27
-
-
0030742588
-
The RHD gene is highly detectable in RhD-negative japanese donors
-
Okuda H, Kawano M, Iwamoto S, Tanaka M, Seno T, Okuba Y, Kajii E. 1997. The RHD gene is highly detectable in RhD-negative Japanese donors. J Clin Invest 100: 373.
-
(1997)
J Clin Invest
, vol.100
, pp. 373
-
-
Okuda, H.1
Kawano, M.2
Iwamoto, S.3
Tanaka, M.4
Seno, T.5
Okuba, Y.6
Kajii, E.7
-
29
-
-
0029967852
-
DNA-based Rhesus typing: Simultaneously determination of RHC and RHD status using the polymerase chain reaction
-
Poulter M, Kemp TJ, Carritt B. 1996. DNA-based Rhesus typing: simultaneously determination of RHC and RHD status using the polymerase chain reaction. Vox Sang 70: 164-168.
-
(1996)
Vox Sang
, vol.70
, pp. 164-168
-
-
Poulter, M.1
Kemp, T.J.2
Carritt, B.3
-
30
-
-
0030982624
-
Prenatal analysis of rhesus CcDEe blood groups by heteroduplex generator
-
Rose NC, Hurwitz C, Silberstein L, Andovalu R, Stoerker J. 1997. Prenatal analysis of rhesus CcDEe blood groups by heteroduplex generator. Am J Obstet Gynecol 176: 1084-1089.
-
(1997)
Am J Obstet Gynecol
, vol.176
, pp. 1084-1089
-
-
Rose, N.C.1
Hurwitz, C.2
Silberstein, L.3
Andovalu, R.4
Stoerker, J.5
-
31
-
-
0028003895
-
The use of polymerase chain reaction to determine fetal RhD status
-
Rossiter JP, Blakemore KJ, Kickler TS, Kasch LM, Khourami AN, Pressman EK, Sciscione AC, Kazazian HH. 1994. The use of polymerase chain reaction to determine fetal RhD status. Am J Obstet Gynecol 171: 1047-1051.
-
(1994)
Am J Obstet Gynecol
, vol.171
, pp. 1047-1051
-
-
Rossiter, J.P.1
Blakemore, K.J.2
Kickler, T.S.3
Kasch, L.M.4
Khourami, A.N.5
Pressman, E.K.6
Sciscione, A.C.7
Kazazian, H.H.8
-
32
-
-
0343836467
-
Molecular basis of the lack of expression of some Rh epitopes in D category phenotypes
-
Rouillac C, Mouro I, Beolet M, Cartron JP, Le Van Kim C. Colin Y. 1994, Molecular basis of the lack of expression of some Rh epitopes in D category phenotypes. Br J Haemat 87 (Suppl 1): 150.
-
(1994)
Br J Haemat
, vol.87
, Issue.SUPPL. 1
, pp. 150
-
-
Rouillac, C.1
Mouro, I.2
Beolet, M.3
Cartron, J.P.4
Le Van Kim, C.5
Colin, Y.6
-
33
-
-
0029059940
-
Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alterations of D epitopes
-
Rouillac C, Colin Y, Hughes-Jones NC, Beolet M, d'Ambrioso AM, Cartron J-P, Le van Kim C. 1995a. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alterations of D epitopes. Blood 85: 2937-2944.
-
(1995)
Blood
, vol.85
, pp. 2937-2944
-
-
Rouillac, C.1
Colin, Y.2
Hughes-Jones, N.C.3
Beolet, M.4
D'Ambrioso, A.M.5
Cartron, J.-P.6
Le Van Kim, C.7
-
34
-
-
0028963904
-
Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes
-
Rouillac C, Le Van Kim C, Blancher A, Roubinet F, Cartron JP, Colin Y. 1995b. Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes. Br J Haemat 89: 424-426.
-
(1995)
Br J Haemat
, vol.89
, pp. 424-426
-
-
Rouillac, C.1
Le Van Kim, C.2
Blancher, A.3
Roubinet, F.4
Cartron, J.P.5
Colin, Y.6
-
37
-
-
0029066655
-
Rapid RhD genotyping by polymerase chain reaction-based amplification of DNA
-
Simsek S, Faas BHW, Bleeker PMM, Overbeeke MAM, Cuỳpers TH, van der Schoot CE, van dem Borne AEGKR. 1995. Rapid RhD genotyping by polymerase chain reaction-based amplification of DNA. Blood 85: 2975-2980.
-
(1995)
Blood
, vol.85
, pp. 2975-2980
-
-
Simsek, S.1
Faas, B.H.W.2
Bleeker, P.M.M.3
Overbeeke, M.A.M.4
Cuỳpers, T.H.5
Van Der Schoot, C.E.6
Van Dem Borne, A.E.G.K.R.7
-
38
-
-
0028804663
-
Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease
-
Spence WC, Maddalena A, Demers DB, Bick DP. 1995. Molecular analysis of the RhD genotype in fetuses at risk for RhD hemolytic disease. Obstet Gynecol 85: 296-298.
-
(1995)
Obstet Gynecol
, vol.85
, pp. 296-298
-
-
Spence, W.C.1
Maddalena, A.2
Demers, D.B.3
Bick, D.P.4
-
39
-
-
0030007133
-
Heteroduplex generator in analysis of Rh blood group alleles
-
Stoerker J, Hurwitz C, Rose NC, Silberstein LE, Highsmith WE. 1996. Heteroduplex generator in analysis of Rh blood group alleles. Clin Chem 42: 356-360.
-
(1996)
Clin Chem
, vol.42
, pp. 356-360
-
-
Stoerker, J.1
Hurwitz, C.2
Rose, N.C.3
Silberstein, L.E.4
Highsmith, W.E.5
-
40
-
-
0029915140
-
Prenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction
-
Van Den Veyver IB, Subramanian SB, Hudson KM, Werch J, Moise KJ, Hughes MR. 1996. Prenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction. Obster Gynecol 87: 419-422.
-
(1996)
Obster Gynecol
, vol.87
, pp. 419-422
-
-
Van Den Veyver, I.B.1
Subramanian, S.B.2
Hudson, K.M.3
Werch, J.4
Moise, K.J.5
Hughes, M.R.6
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