-
1
-
-
0014217230
-
Prevention of Rh-hemolytic disease
-
Clarke CA. Prevention of Rh-hemolytic disease. Br Med J 1967;4:484-5.
-
(1967)
Br Med J
, vol.4
, pp. 484-485
-
-
Clarke, C.A.1
-
2
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997;350:485-7.
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
-
3
-
-
0032506669
-
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
-
Lo YM, Hjelm NM, Fidler C, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 1998;339:1734-8.
-
(1998)
N Engl J Med
, vol.339
, pp. 1734-1738
-
-
Lo, Y.M.1
Hjelm, N.M.2
Fidler, C.3
-
4
-
-
84891558107
-
Medical genetics: advances in brief: presence of fetal DNA in maternal plasma and serum
-
Barnicoat A. Medical genetics: advances in brief: presence of fetal DNA in maternal plasma and serum. J Med Genet 1998;35:345.
-
(1998)
J Med Genet
, vol.35
, pp. 345
-
-
Barnicoat, A.1
-
5
-
-
0032855554
-
Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21
-
Lo YM, Lau TK, Zhang J, et al. Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21. Clin Chem 1999;45:1747-51.
-
(1999)
Clin Chem
, vol.45
, pp. 1747-1751
-
-
Lo, Y.M.1
Lau, T.K.2
Zhang, J.3
-
6
-
-
0036692036
-
Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service
-
Finning KM, Martin PG, Soothill PW, et al. Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service. Transfusion 2002;42:1079-85.
-
(2002)
Transfusion
, vol.42
, pp. 1079-1085
-
-
Finning, K.M.1
Martin, P.G.2
Soothill, P.W.3
-
7
-
-
3242691320
-
A clinical service in the UK to predict fetal Rh (Rhesus) D blood group using free fetal DNA in maternal plasma
-
Finning K, Martin P, Daniels G. A clinical service in the UK to predict fetal Rh (Rhesus) D blood group using free fetal DNA in maternal plasma. Ann N Y Acad Sci 2004;1022:119-23.
-
(2004)
Ann N Y Acad Sci
, vol.1022
, pp. 119-123
-
-
Finning, K.1
Martin, P.2
Daniels, G.3
-
8
-
-
33748787168
-
Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood-a meta-analysis
-
Geifman-Holtzman O, Grotegut CA, Gaughan JP. Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood-a meta-analysis. Am J Obstet Gynecol 2006;195:1163-73.
-
(2006)
Am J Obstet Gynecol
, vol.195
, pp. 1163-1173
-
-
Geifman-Holtzman, O.1
Grotegut, C.A.2
Gaughan, J.P.3
-
9
-
-
69249236998
-
Evaluation of non-invasive prenatal RHD genotyping of the fetus
-
Hyland CA, Gardener GJ, Davies H, et al. Evaluation of non-invasive prenatal RHD genotyping of the fetus. Med J Aust 2009;191:21-5.
-
(2009)
Med J Aust
, vol.191
, pp. 21-25
-
-
Hyland, C.A.1
Gardener, G.J.2
Davies, H.3
-
10
-
-
84868142445
-
Management and prevention of red cell alloimmunization in pregnancy: a systematic review
-
Moise KJ, Jr., Argoti PS. Management and prevention of red cell alloimmunization in pregnancy: a systematic review. Obstet Gynecol 2012;120:1132-9.
-
(2012)
Obstet Gynecol
, vol.120
, pp. 1132-1139
-
-
Moise Jr., K.J.1
Argoti, P.S.2
-
11
-
-
42249108710
-
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study
-
Finning K, Martin P, Summers J, et al. Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study. BMJ 2008;336:816-8.
-
(2008)
BMJ
, vol.336
, pp. 816-818
-
-
Finning, K.1
Martin, P.2
Summers, J.3
-
12
-
-
84859757903
-
Report of the first nationally implemented clinical routine screening for fetal RHD in D- pregnant women to ascertain the requirement for antenatal RhD prophylaxis
-
Clausen FB, Christiansen M, Steffensen R, et al. Report of the first nationally implemented clinical routine screening for fetal RHD in D- pregnant women to ascertain the requirement for antenatal RhD prophylaxis. Transfusion 2012;52:752-8.
-
(2012)
Transfusion
, vol.52
, pp. 752-758
-
-
Clausen, F.B.1
Christiansen, M.2
Steffensen, R.3
-
13
-
-
84864288916
-
Noninvasive single-exon fetal RHD determination in a routine screening program in early pregnancy
-
Wikman AT, Tiblad E, Karlsson A, et al. Noninvasive single-exon fetal RHD determination in a routine screening program in early pregnancy. Obstet Gynecol 2012;120:227-34.
-
(2012)
Obstet Gynecol
, vol.120
, pp. 227-234
-
-
Wikman, A.T.1
Tiblad, E.2
Karlsson, A.3
-
14
-
-
84891561486
-
Noninvasive prenatal screening for RHD in the Netherlands: one test for targeted antenatal and postnatal anti-D prophylaxis
-
de Haas M, Van der Schoot C, van der Ploeg C, et al. Noninvasive prenatal screening for RHD in the Netherlands: one test for targeted antenatal and postnatal anti-D prophylaxis. Vox Sang 2012;103:33.
-
(2012)
Vox Sang
, vol.103
, pp. 33
-
-
de Haas, M.1
Van der Schoot, C.2
van der Ploeg, C.3
-
15
-
-
67651120044
-
Red cell genotyping and the future of pretransfusion testing
-
Anstee DJ. Red cell genotyping and the future of pretransfusion testing. Blood 2009;114:248-56.
-
(2009)
Blood
, vol.114
, pp. 248-256
-
-
Anstee, D.J.1
-
16
-
-
0025723965
-
Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis
-
Colin Y, Cherif-Zahar B, Le Van Kim C, et al. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 1991;78:2747-52.
-
(1991)
Blood
, vol.78
, pp. 2747-2752
-
-
Colin, Y.1
Cherif-Zahar, B.2
Le Van Kim, C.3
-
17
-
-
84928201868
-
Rh Blood Group System
-
Daniels G (ed.). Oxford: Blackwell Publishing Company
-
Daniels G. Rh Blood Group System. In Human Blood Groups, Daniels G (ed.). Oxford: Blackwell Publishing Company, 2002;195-274.
-
(2002)
Human Blood Groups
, pp. 195-274
-
-
Daniels, G.1
-
19
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas BH, Beckers EA, Wildoer P, et al. Molecular background of VS and weak C expression in blacks. Transfusion 1997;37:38-44.
-
(1997)
Transfusion
, vol.37
, pp. 38-44
-
-
Faas, B.H.1
Beckers, E.A.2
Wildoer, P.3
-
20
-
-
0033957696
-
The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype
-
Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 2000;95:12-8.
-
(2000)
Blood
, vol.95
, pp. 12-18
-
-
Singleton, B.K.1
Green, C.A.2
Avent, N.D.3
-
21
-
-
84876794954
-
Variants of RhD-current testing and clinical consequences
-
Daniels G. Variants of RhD-current testing and clinical consequences. Br J Haematol 2013;161:461-70.
-
(2013)
Br J Haematol
, vol.161
, pp. 461-470
-
-
Daniels, G.1
-
22
-
-
0034651012
-
The Rh blood group system: a review
-
Avent ND, Reid ME. The Rh blood group system: a review. Blood 2000;95:375-87.
-
(2000)
Blood
, vol.95
, pp. 375-387
-
-
Avent, N.D.1
Reid, M.E.2
-
23
-
-
0012514010
-
Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese
-
Shao CP, Maas JH, Su YQ, et al. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese. Vox Sang 2002;83:156-61.
-
(2002)
Vox Sang
, vol.83
, pp. 156-161
-
-
Shao, C.P.1
Maas, J.H.2
Su, Y.Q.3
-
24
-
-
1442275829
-
Review: the molecular basis of the Rh blood group phenotypes
-
Wagner FF, Flegel WA. Review: the molecular basis of the Rh blood group phenotypes. Immunohematology 2004;20:23-36.
-
(2004)
Immunohematology
, vol.20
, pp. 23-36
-
-
Wagner, F.F.1
Flegel, W.A.2
-
25
-
-
84891559313
-
-
Rhesus Base: D negative and DEL alleles [WWW document],[accessed on 4 July ].
-
Wagner F. Rhesus Base: D negative and DEL alleles [WWW document] http://www.uni-ulm.de/~fwagner/RH/RB/neg.htm [accessed on 4 July 2013].
-
(2013)
-
-
Wagner, F.1
-
26
-
-
84934434964
-
RHD genotyping from maternal plasma: guidelines and technical challenges
-
Avent ND. RHD genotyping from maternal plasma: guidelines and technical challenges. Methods Mol Biol 2008;444:185-201.
-
(2008)
Methods Mol Biol
, vol.444
, pp. 185-201
-
-
Avent, N.D.1
-
27
-
-
33751362129
-
Evaluation of prenatal RHD typing strategies on cell-free fetal DNA from maternal plasma
-
Grootkerk-Tax MG, Soussan AA, de Haas M, et al. Evaluation of prenatal RHD typing strategies on cell-free fetal DNA from maternal plasma. Transfusion 2006;46:2142-8.
-
(2006)
Transfusion
, vol.46
, pp. 2142-2148
-
-
Grootkerk-Tax, M.G.1
Soussan, A.A.2
de Haas, M.3
-
28
-
-
80052714987
-
Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience
-
Scheffer P, van der Schoot C, Page-Christiaens G, et al. Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience. BJOG 2011; 108:1340-8.
-
(2011)
BJOG
, vol.108
, pp. 1340-1348
-
-
Scheffer, P.1
van der Schoot, C.2
Page-Christiaens, G.3
-
29
-
-
34250671892
-
Blood group genotyping in Germany
-
Flegel WA. Blood group genotyping in Germany. Transfusion 2007;47:47S-53S.
-
(2007)
Transfusion
, vol.47
-
-
Flegel, W.A.1
-
30
-
-
0028241841
-
Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r'r') phenotypes
-
Hyland CA, Wolter LC, Saul A. Three unrelated RhD gene polymorphisms identified among blood donors with Rhesus CCee (r'r') phenotypes. Blood 1994;84:321-4.
-
(1994)
Blood
, vol.84
, pp. 321-324
-
-
Hyland, C.A.1
Wolter, L.C.2
Saul, A.3
-
31
-
-
0032755410
-
Fetal RhD genotyping from maternal plasma
-
Lo YM. Fetal RhD genotyping from maternal plasma. Ann Med 1999;31:308-12.
-
(1999)
Ann Med
, vol.31
, pp. 308-312
-
-
Lo, Y.M.1
-
32
-
-
67650262318
-
The Bloodgen project of the European Union
-
Avent ND on behalf of the Bloodgen consortium. In, Scharf R (ed.). Düsseldorf: Karger
-
Avent ND on behalf of the Bloodgen consortium. The Bloodgen project of the European Union. In Progress and Challenges in Transfusion Medicine, Hemostasis, and Hemotherapy, Scharf R (ed.). Düsseldorf: Karger, 2008;178-88.
-
(2008)
Progress and Challenges in Transfusion Medicine, Hemostasis, and Hemotherapy
, pp. 178-188
-
-
-
33
-
-
84865740742
-
Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype
-
Gardener GJ, Legler TJ, Hyett JA, et al. Anti-D in pregnant women with the RHD(IVS3+1G>A)-associated DEL phenotype. Transfusion 2012;52:2016-9.
-
(2012)
Transfusion
, vol.52
, pp. 2016-2019
-
-
Gardener, G.J.1
Legler, T.J.2
Hyett, J.A.3
-
34
-
-
27744575730
-
A comprehensive analysis of DEL types: partial DEL individuals are prone to anti-D alloimmunization
-
Kormoczi GF, Gassner C, Shao CP, et al. A comprehensive analysis of DEL types: partial DEL individuals are prone to anti-D alloimmunization. Transfusion 2005;45:1561-7.
-
(2005)
Transfusion
, vol.45
, pp. 1561-1567
-
-
Kormoczi, G.F.1
Gassner, C.2
Shao, C.P.3
-
35
-
-
77950542574
-
Immunogenicity reloaded
-
Flegel WA. Immunogenicity reloaded. Blood 2009;114:3979-80.
-
(2009)
Blood
, vol.114
, pp. 3979-3980
-
-
Flegel, W.A.1
-
36
-
-
0034656006
-
Weak D alleles express distinct phenotypes
-
Wagner FF, Frohmajer A, Ladewig B, et al. Weak D alleles express distinct phenotypes. Blood 2000;95:2699-708.
-
(2000)
Blood
, vol.95
, pp. 2699-2708
-
-
Wagner, F.F.1
Frohmajer, A.2
Ladewig, B.3
-
37
-
-
55349139320
-
Applying molecular immunohematology discoveries to standards of practice in blood banks: now is the time
-
Denomme GA, Flegel WA. Applying molecular immunohematology discoveries to standards of practice in blood banks: now is the time. Transfusion 2008;48:2461-75.
-
(2008)
Transfusion
, vol.48
, pp. 2461-2475
-
-
Denomme, G.A.1
Flegel, W.A.2
-
38
-
-
78049467018
-
Antenatal Rh prophylaxis is unnecessary for " Asia type" DEL women
-
Shao CP, Xu H, Xu Q, et al. Antenatal Rh prophylaxis is unnecessary for " Asia type" DEL women. Transfus Clin Biol 2010;17:260-4.
-
(2010)
Transfus Clin Biol
, vol.17
, pp. 260-264
-
-
Shao, C.P.1
Xu, H.2
Xu, Q.3
-
39
-
-
76149127039
-
Transfusion of RhD-positive blood in " Asia type" DEL recipients
-
Shao CP. Transfusion of RhD-positive blood in "Asia type" DEL recipients. N Engl J Med 2010;362:472-3.
-
(2010)
N Engl J Med
, vol.362
, pp. 472-473
-
-
Shao, C.P.1
-
40
-
-
77952312473
-
Aberrant RNA splicing in RHD 7-9 exons of DEL individuals in Taiwan: a mechanism study
-
Liu HC, Eng HL, Yang YF, et al. Aberrant RNA splicing in RHD 7-9 exons of DEL individuals in Taiwan: a mechanism study. Biochim Biophys Acta 2010;1800:565-73.
-
(2010)
Biochim Biophys Acta
, vol.1800
, pp. 565-573
-
-
Liu, H.C.1
Eng, H.L.2
Yang, Y.F.3
|