-
1
-
-
10344262881
-
Fetal blood group genotyping from DNA from maternal plasma: An important advance in the management and prevention of haemolytic disease of the fetus and newborn
-
Daniels G, Finning K, Martin P, Soothill P. Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn. Vox Sang 2004 87 : 225 32.
-
(2004)
Vox Sang
, vol.87
, pp. 225-32
-
-
Daniels, G.1
Finning, K.2
Martin, P.3
Soothill, P.4
-
2
-
-
33751362129
-
Evaluation of prenatal RHD typing strategies on cell-free fetal DNA from maternal plasma
-
Grootkerk-Tax MG, Soussan AA, de Haas M, Maaskant-van Wijk PA, van der Schoot CE. Evaluation of prenatal RHD typing strategies on cell-free fetal DNA from maternal plasma. Transfusion 2006 46 : 2142 8.
-
(2006)
Transfusion
, vol.46
, pp. 2142-8
-
-
Grootkerk-Tax, M.G.1
Soussan, A.A.2
De Haas, M.3
Maaskant-Van Wijk, P.A.4
Van Der Schoot, C.E.5
-
3
-
-
14844304701
-
Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RhD-negative pregnancies
-
Hromadnikova I, Vechetova L, Vesela K, Benesova B, Doucha J, Vlk R. Non-invasive fetal RHD and RHCE genotyping using real-time PCR testing of maternal plasma in RhD-negative pregnancies. J Histochem Cytochem 2005 53 : 301 5.
-
(2005)
J Histochem Cytochem
, vol.53
, pp. 301-5
-
-
Hromadnikova, I.1
Vechetova, L.2
Vesela, K.3
Benesova, B.4
Doucha, J.5
Vlk, R.6
-
4
-
-
3342986296
-
Large-scale pre-diagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women
-
DOI 10.2165/00066982-200408010-00004
-
Rouillac-Le Sciellour C, Puillandre P, Gillot R, Baulard C, Métral S, Le Van Kim C et al. Large-scale pre-diagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women. Mol Diagn 2004 8 : 23 31. (Pubitemid 38989470)
-
(2004)
Molecular Diagnosis
, vol.8
, Issue.1
, pp. 23-31
-
-
Rouillac-Le Sciellour, C.1
Puillandre, P.2
Gillot, R.3
Baulard, C.4
Metral, S.5
Le Van Kim, C.6
Cartron, J.-P.7
Colin, Y.8
Brossard, Y.9
-
5
-
-
26944483571
-
Noninvasive determination of fetal RHD status by examination of cell-free DNA in maternal plasma
-
Brojer E, Zupanska B, Guz K, Orziñska A, Kaliñska A. Noninvasive determination of fetal RHD status by examination of cell-free DNA in maternal plasma. Transfusion 2005 45 : 1473 80.
-
(2005)
Transfusion
, vol.45
, pp. 1473-80
-
-
Brojer, E.1
Zupanska, B.2
Guz, K.3
Orziñska, A.4
Kaliñska, A.5
-
6
-
-
28544450725
-
Reliable test for prenatal prediction of fetal RhD type using maternal plasma from RhD negative women
-
Clausen FB, Krog GR, Rieneck K, Nielsen LK, Lundquist R, Finning K et al. Reliable test for prenatal prediction of fetal RhD type using maternal plasma from RhD negative women. Prenat Diagn 2005 25 : 1040 4.
-
(2005)
Prenat Diagn
, vol.25
, pp. 1040-4
-
-
Clausen, F.B.1
Krog, G.R.2
Rieneck, K.3
Nielsen, L.K.4
Lundquist, R.5
Finning, K.6
-
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. 119-23
-
-
Finning, K.1
Martin, P.2
Daniels, G.3
-
8
-
-
0343081096
-
Genetic polymorphism of RhD-negative associated haplotypes in the Chinese
-
Lan JC, Chen Q, Wu DL, Ding H, Pong DB, Zhao T. Genetic polymorphism of RhD-negative associated haplotypes in the Chinese. J Hum Genet 2000 45 : 224 7.
-
(2000)
J Hum Genet
, vol.45
, pp. 224-7
-
-
Lan, J.C.1
Chen, Q.2
Wu, D.L.3
Ding, H.4
Pong, D.B.5
Zhao, T.6
-
9
-
-
33847081122
-
Molecular basis of D variants in Chinese person
-
Yan LY, Wu JJ, Zhu FM, Hong X, Xu X. Molecular basis of D variants in Chinese person. Transfusion 2007 47 : 471 7.
-
(2007)
Transfusion
, vol.47
, pp. 471-7
-
-
Yan, L.Y.1
Wu, J.J.2
Zhu, F.M.3
Hong, X.4
Xu, X.5
-
10
-
-
33847683704
-
Molecular and family analyses revealed two novel RHD alleles in a survey of a Chinese RhD-negative population
-
Ye LY, Guo ZH, Li Q, Zhu ZY. Molecular and family analyses revealed two novel RHD alleles in a survey of a Chinese RhD-negative population. Vox Sang 2007 92 : 242 6.
-
(2007)
Vox Sang
, vol.92
, pp. 242-6
-
-
Ye, L.Y.1
Guo, Z.H.2
Li, Q.3
Zhu, Z.Y.4
-
11
-
-
0141976657
-
Molecular basis for the RhD negative phenotype in Chinese
-
Peng CT, Shih MC, Liu TC, Lin IL, Jaung SJ, Chang JG. Molecular basis for the RhD negative phenotype in Chinese. Int J Mol Med 2003 11 : 515 21.
-
(2003)
Int J Mol Med
, vol.11
, pp. 515-21
-
-
Peng, C.T.1
Shih, M.C.2
Liu, T.C.3
Lin, I.L.4
Jaung, S.J.5
Chang, J.G.6
-
12
-
-
0037274019
-
Analysis of RHD genes in Taiwanese RhD-negative donors by the multiplex PCR method
-
Lee YL, Chiou HL, Hu SN, Wang L. Analysis of RHD genes in Taiwanese RhD-negative donors by the multiplex PCR method. J Clin Lab Anal 2003 17 : 80 4.
-
(2003)
J Clin Lab Anal
, vol.17
, pp. 80-4
-
-
Lee, Y.L.1
Chiou, H.L.2
Hu, S.N.3
Wang, L.4
-
13
-
-
2442477666
-
A new hybrid RHD-positive, D antigen-negative allele
-
Shao CP, Xiong W. A new hybrid RHD-positive, D antigen-negative allele. Transfus Med 2004 14 : 185 6.
-
(2004)
Transfus Med
, vol.14
, pp. 185-6
-
-
Shao, C.P.1
Xiong, W.2
-
14
-
-
13444265943
-
Systemic analysis and zygosity determination of the RHD gene in a D-negative Chinese Han population reveals a novel D-negative RHD gene
-
Xu Q, Grootkerk-Tax MG, Maaskant-van Wijk PA, van der Schoot CE. Systemic analysis and zygosity determination of the RHD gene in a D-negative Chinese Han population reveals a novel D-negative RHD gene. Vox Sang 2005 88 : 35 40.
-
(2005)
Vox Sang
, vol.88
, pp. 35-40
-
-
Xu, Q.1
Grootkerk-Tax, M.G.2
Maaskant-Van Wijk, P.A.3
Van Der Schoot, C.E.4
-
15
-
-
0037085782
-
RHCE represents the ancestral RH position, while RHD is the duplicated gene
-
Wagner FF, Flegel WA. RHCE represents the ancestral RH position, while RHD is the duplicated gene. Blood 2002 99 : 2272 3.
-
(2002)
Blood
, vol.99
, pp. 2272-3
-
-
Wagner, F.F.1
Flegel, W.A.2
-
16
-
-
0027180212
-
Molecular genetic basis of the human Rhesus blood group system
-
Mouro I, Colin Y, Cherif-Zahar B, Cartron JP, Le Van Kim C. Molecular genetic basis of the human Rhesus blood group system. Nat Genet 1993 5 : 62 5.
-
(1993)
Nat Genet
, vol.5
, pp. 62-5
-
-
Mouro, I.1
Colin, Y.2
Cherif-Zahar, B.3
Cartron, J.P.4
Le Van Kim, C.5
-
17
-
-
0034659823
-
RHD gene deletion occurred in the Rhesus box
-
Wagner FF, Flegel WA. RHD gene deletion occurred in the Rhesus box. Blood 2000 95 : 3662 8.
-
(2000)
Blood
, vol.95
, pp. 3662-8
-
-
Wagner, F.F.1
Flegel, W.A.2
-
18
-
-
0035057567
-
Determination of RhD zygosity: Comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach
-
Chiu RW, Murphy MF, Fidler C, Zee BC, Wainscoat JS, Lo YM. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2001 47 : 667 72.
-
(2001)
Clin Chem
, vol.47
, pp. 667-72
-
-
Chiu, R.W.1
Murphy, M.F.2
Fidler, C.3
Zee, B.C.4
Wainscoat, J.S.5
Lo, Y.M.6
-
19
-
-
15244348983
-
High variability of the RH locus in different ethnic backgrounds
-
Avent ND. High variability of the RH locus in different ethnic backgrounds. Transfusion 2005 45 : 293 4.
-
(2005)
Transfusion
, vol.45
, pp. 293-4
-
-
Avent, N.D.1
-
20
-
-
0032932817
-
Molecular basis of weak D phenotypes
-
Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999 93 : 385 93.
-
(1999)
Blood
, vol.93
, pp. 385-93
-
-
Wagner, F.F.1
Gassner, C.2
Müller, T.H.3
Schönitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
21
-
-
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. 375-87
-
-
Avent, N.D.1
Reid, M.E.2
-
22
-
-
0033957696
-
The presence of an RHD pseudogene containing a 37 bp duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype
-
Singleton BK, Green CA, Avent ND, Martin PG, Smart E, Daka A et al. The presence of an RHD pseudogene containing a 37 bp 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. 12-8
-
-
Singleton, B.K.1
Green, C.A.2
Avent, N.D.3
Martin, P.G.4
Smart, E.5
Daka, A.6
-
25
-
-
0030610066
-
Further analysis of Del (D-eluate) using polymerase chain reaction (PCR) with RHD gene-specific primers
-
Fukumori Y, Hori Y, Ohnoki S, Nagao N, Shibata H, Okubo Y et al. Further analysis of Del (D-eluate) using polymerase chain reaction (PCR) with RHD gene-specific primers. Transfus Med 1997 7 : 227 31.
-
(1997)
Transfus Med
, vol.7
, pp. 227-31
-
-
Fukumori, Y.1
Hori, Y.2
Ohnoki, S.3
Nagao, N.4
Shibata, H.5
Okubo, Y.6
-
26
-
-
17044380221
-
Anti-D immunization by Del red blood cells
-
Wagner T, Körmöczi GF, Buchta C, Vadon M, Lanzer G, Mayr WR et al. Anti-D immunization by Del red blood cells. Transfusion 2005 45 : 520 6.
-
(2005)
Transfusion
, vol.45
, pp. 520-6
-
-
Wagner, T.1
Körmöczi, G.F.2
Buchta, C.3
Vadon, M.4
Lanzer, G.5
Mayr, W.R.6
-
27
-
-
20144388742
-
Presence of RHD in serologically D-,C/E+ individuals: A European multicenter study
-
Gassner C, Doescher A, Drnovsek TD, Rozman P, Eicher NI, Legler TJ et al. Presence of RHD in serologically D-,C/E+ individuals: a European multicenter study. Transfusion 2005 45 : 527 38.
-
(2005)
Transfusion
, vol.45
, pp. 527-38
-
-
Gassner, C.1
Doescher, A.2
Drnovsek, T.D.3
Rozman, P.4
Eicher, N.I.5
Legler, T.J.6
-
28
-
-
0032173426
-
Human RhDel is caused by a deletion of 1013 bp between introns 8 and 9 including exon 9 of RHD gene
-
Chang JG, Wang JC, Yang TY, Tsan KW, Shih MC, Peng CT et al. Human RhDel is caused by a deletion of 1013 bp between introns 8 and 9 including exon 9 of RHD gene. Blood 1998 92 : 2602 4.
-
(1998)
Blood
, vol.92
, pp. 2602-4
-
-
Chang, J.G.1
Wang, J.C.2
Yang, T.Y.3
Tsan, K.W.4
Shih, M.C.5
Peng, C.T.6
-
29
-
-
3242760515
-
RHD1227A is an important genetic marker for RhD(el) individuals
-
Chen JC, Lin TM, Chen YL, Wang YH, Jin YT, Yue CT. RHD1227A is an important genetic marker for RhD(el) individuals. Am J Clin Pathol 2004 122 : 193 8.
-
(2004)
Am J Clin Pathol
, vol.122
, pp. 193-8
-
-
Chen, J.C.1
Lin, T.M.2
Chen, Y.L.3
Wang, Y.H.4
Jin, Y.T.5
Yue, C.T.6
-
30
-
-
0037341393
-
Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination
-
Hromadnikova I, Houbova B, Hridelova D, Voslarova S, Kofer J, Komrska V et al. Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination. Prenat Diagn 2003 23 : 235 8.
-
(2003)
Prenat Diagn
, vol.23
, pp. 235-8
-
-
Hromadnikova, I.1
Houbova, B.2
Hridelova, D.3
Voslarova, S.4
Kofer, J.5
Komrska, V.6
-
31
-
-
0036692036
-
Prediction of fetal D status from maternal plasma: Introduction of a new noninvasive fetal RHD genotyping service
-
Finning KM, Martin PG, Soothill PW, Avent ND. 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. 1079-85
-
-
Finning, K.M.1
Martin, P.G.2
Soothill, P.W.3
Avent, N.D.4
-
32
-
-
0036889722
-
Prediction of fetal RhD and RhCcEe phenotype from maternal plasma with real-time polymerase chain reaction
-
Legler TJ, Lynen R, Maas JH, Pindur G, Kulenkampff D, Suren A et al. Prediction of fetal RhD and RhCcEe phenotype from maternal plasma with real-time polymerase chain reaction. Transfus Apher Sci 2002 27 : 217 23.
-
(2002)
Transfus Apher Sci
, vol.27
, pp. 217-23
-
-
Legler, T.J.1
Lynen, R.2
Maas, J.H.3
Pindur, G.4
Kulenkampff, D.5
Suren, A.6
-
33
-
-
0032506669
-
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
-
Lo YM, Hjelm NM, Fidler C, Sargent IL, Murphy MF, Chamberlain PF 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. 1734-8
-
-
Lo, Y.M.1
Hjelm, N.M.2
Fidler, C.3
Sargent, I.L.4
Murphy, M.F.5
Chamberlain, P.F.6
-
34
-
-
20944449591
-
Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma
-
Hromadnikova I, Vechetova L, Vesela K, Benesova B, Doucha J, Kulovany E et al. Non-invasive fetal RHD exon 7 and exon 10 genotyping using real-time PCR testing of fetal DNA in maternal plasma. Fetal Diagn Ther 2005 20 : 275 80.
-
(2005)
Fetal Diagn Ther
, vol.20
, pp. 275-80
-
-
Hromadnikova, I.1
Vechetova, L.2
Vesela, K.3
Benesova, B.4
Doucha, J.5
Kulovany, E.6
-
35
-
-
0037225919
-
Prenatal typing of Rh and Kell blood group system antigens: The edge of a watershed
-
DOI 10.1053/tmrv.2003.50001
-
van der Schoot CE, Tax GH, Rijnders RJ, de Haas M, Christiaens GC. Prenatal typing of Rh and kell blood group system antigens: the edge of a watershed. Transfus Med Rev 2003 17 : 31 44. (Pubitemid 36042643)
-
(2003)
Transfusion Medicine Reviews
, vol.17
, Issue.1
, pp. 31-44
-
-
Van Der Schoot, C.E.1
Tax, G.H.M.2
Rijnders, R.J.P.3
De Haas, M.4
Christiaens, G.C.M.L.5
-
37
-
-
28444448441
-
Noninvasive prenatal RHD genotyping by real-time polymerase chain reaction using plasma from D-negative pregnant women
-
Zhou L, Thorson JA, Nugent C, Davenport RD, Butch SH, Judd WJ. Noninvasive prenatal RHD genotyping by real-time polymerase chain reaction using plasma from D-negative pregnant women. Am J Obstet Gynecol 2005 193 : 1966 71.
-
(2005)
Am J Obstet Gynecol
, vol.193
, pp. 1966-71
-
-
Zhou, L.1
Thorson, J.A.2
Nugent, C.3
Davenport, R.D.4
Butch, S.H.5
Judd, W.J.6
-
38
-
-
33748566277
-
Fetal RHD genotyping from maternal plasma in a population with a highly diverse ethnic background
-
Machado IN, Castilho L, Pellegrino J Jr., Barini R. Fetal RHD genotyping from maternal plasma in a population with a highly diverse ethnic background. Rev Assoc Med Bras 2006 52 : 232 5.
-
(2006)
Rev Assoc Med Bras
, vol.52
, pp. 232-5
-
-
MacHado, I.N.1
Castilho, L.2
Pellegrino Jr., J.3
Barini, R.4
-
39
-
-
0012514010
-
Molecular background of RhD positive, D-negative, D(el) and weak D phenotypes in Chinese
-
Shao CP, Maas JH, Su YQ, Köhler M, Legler TJ. Molecular background of RhD positive, D-negative, D(el) and weak D phenotypes in Chinese. Vox Sang 2002 83 : 156 61.
-
(2002)
Vox Sang
, vol.83
, pp. 156-61
-
-
Shao, C.P.1
Maas, J.H.2
Su, Y.Q.3
Köhler, M.4
Legler, T.J.5
-
40
-
-
0032521490
-
Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features
-
Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998 91 : 2157 68.
-
(1998)
Blood
, vol.91
, pp. 2157-68
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
Schonitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
41
-
-
15244361715
-
Molecular characterization of D-Korean persons: Development of a diagnostic strategy
-
Kim JY, Kim SY, Kim CA, Yon GS, Park SS. Molecular characterization of D-Korean persons: development of a diagnostic strategy. Transfusion 2005 45 : 345 52.
-
(2005)
Transfusion
, vol.45
, pp. 345-52
-
-
Kim, J.Y.1
Kim, S.Y.2
Kim, C.A.3
Yon, G.S.4
Park, S.S.5
|