-
1
-
-
0034007375
-
RhD haemolytic disease of the fetus and the newborn
-
Urbaniak, S. J. and Greiss, M. A. (2000) RhD haemolytic disease of the fetus and the newborn. Blood Rev. 14, 44-61.
-
(2000)
Blood Rev
, vol.14
, pp. 44-61
-
-
Urbaniak, S.J.1
Greiss, M.A.2
-
2
-
-
0029849701
-
Haemolytic disease of the newborn due to anti-G
-
Hadley, A. G., Poole, G. D., Poole, J., Anderson, N. A., and Robson, M. (1996) Haemolytic disease of the newborn due to anti-G. Vox Sang. 71, 108-112.
-
(1996)
Vox Sang
, vol.71
, pp. 108-112
-
-
Hadley, A.G.1
Poole, G.D.2
Poole, J.3
Anderson, N.A.4
Robson, M.5
-
3
-
-
33745039724
-
Molecular biology of Rh proteins and relevance to molecular medicine
-
Avent, N. D., Madgett, T. E., Lee, Z. E., Head, D. J., Maddocks, D. G., and Skinner, L. H. (2006) Molecular biology of Rh proteins and relevance to molecular medicine. Expert Rev. Mol. Med. 8, 1-20.
-
(2006)
Expert Rev. Mol. Med
, vol.8
, pp. 1-20
-
-
Avent, N.D.1
Madgett, T.E.2
Lee, Z.E.3
Head, D.J.4
Maddocks, D.G.5
Skinner, L.H.6
-
4
-
-
0034651012
-
The Rh blood group system: A review
-
Avent, N. D. and Reid, M. E. (2000) The Rh blood group system: a review. Blood 95, 375-387.
-
(2000)
Blood
, vol.95
, pp. 375-387
-
-
Avent, N.D.1
Reid, M.E.2
-
5
-
-
33644508650
-
Rh proteins: Key structural and functional components of the red cell membrane
-
Van Kim, C. L., Colin, Y., and Cartron, J. P. (2005) Rh proteins: key structural and functional components of the red cell membrane. Blood Rev. 20, 93-110.
-
(2005)
Blood Rev
, vol.20
, pp. 93-110
-
-
Van Kim, C.L.1
Colin, Y.2
Cartron, J.P.3
-
6
-
-
0035053248
-
New insights into the Rh superfamily of genes and proteins in erythroid cells and nonerythroid tissues
-
Huang, C. H. and Liu, P. Z. (2001) New insights into the Rh superfamily of genes and proteins in erythroid cells and nonerythroid tissues. Blood Cells Mol. Dis. 27, 90-101.
-
(2001)
Blood Cells Mol. Dis
, vol.27
, pp. 90-101
-
-
Huang, C.H.1
Liu, P.Z.2
-
7
-
-
1442275829
-
Review: The molecular basis of the Rh blood group phenotypes
-
Wagner, F. F. and Flegel, W. A. (2004) Review: the molecular basis of the Rh blood group phenotypes. Immunohematology 20, 23-36.
-
(2004)
Immunohematology
, vol.20
, pp. 23-36
-
-
Wagner, F.F.1
Flegel, W.A.2
-
8
-
-
7244228186
-
The Rh blood group system in review: A new face for the next decade
-
Westhoff, C. M. (2004) The Rh blood group system in review: a new face for the next decade. Transfusion 44, 1663-1673.
-
(2004)
Transfusion
, vol.44
, pp. 1663-1673
-
-
Westhoff, C.M.1
-
9
-
-
33644803306
-
Modelling the human rhesus proteins: Implications for structure and function
-
Conroy, M. J., Bullough, P. A., Merrick, M., and Avent, N. D. (2005) Modelling the human rhesus proteins: implications for structure and function. Br. J. Haematol. 131, 543-551.
-
(2005)
Br. J. Haematol
, vol.131
, pp. 543-551
-
-
Conroy, M.J.1
Bullough, P.A.2
Merrick, M.3
Avent, N.D.4
-
10
-
-
0034672229
-
Identification of alloreactive T-cell epitopes on the Rhesus D protein
-
Stott, L. M., Barker, R. N., and Urbaniak, S. J. (2000) Identification of alloreactive T-cell epitopes on the Rhesus D protein. Blood 96, 4011-4019.
-
(2000)
Blood
, vol.96
, pp. 4011-4019
-
-
Stott, L.M.1
Barker, R.N.2
Urbaniak, S.J.3
-
11
-
-
14944372972
-
Immune responses and tolerance to the RhD blood group protein in HLA-transgenic mice
-
Hall, A. M., Cairns, L. S., Altmann, D. M., Barker, R. N., and Urbaniak, S. J. (2005) Immune responses and tolerance to the RhD blood group protein in HLA-transgenic mice. Blood 105, 2175-2179.
-
(2005)
Blood
, vol.105
, pp. 2175-2179
-
-
Hall, A.M.1
Cairns, L.S.2
Altmann, D.M.3
Barker, R.N.4
Urbaniak, S.J.5
-
12
-
-
0025024967
-
Molecular cloning and protein structure of a human blood group Rh polypeptide
-
Cherif-Zahar, B., Bloy, C., Van Kim, C. L., et al. (1990) Molecular cloning and protein structure of a human blood group Rh polypeptide. Proc. Natl. Acad. Sci. USA 87, 6243-6247.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 6243-6247
-
-
Cherif-Zahar, B.1
Bloy, C.2
Van Kim, C.L.3
-
13
-
-
0025167261
-
cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression
-
Avent, N. D., Finning, K. M., Martin, P. G., and Soothill, P. W. (1990) cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression. Biochem. J. 271, 821-825.
-
(1990)
Biochem. J
, vol.271
, pp. 821-825
-
-
Avent, N.D.1
Finning, K.M.2
Martin, P.G.3
Soothill, P.W.4
-
14
-
-
0027293541
-
Molecular cloning of RhD cDNA derived derived from a gene present in RhD-positive, but not RhD-negative individuals
-
Arce, M. A., Thompson, E. S., Wagner, S., Coyne, K. E., Ferdmann, B. A., and Lublin, D. M. (1993) Molecular cloning of RhD cDNA derived 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
Ferdmann, B.A.5
Lublin, D.M.6
-
15
-
-
0026495861
-
Molecular cloning and primary structure of the human blood group RhD polypeptide
-
Van Kim, C. L., Mouro. I., Cherif-Zahar, B., et al. (1992) Molecular cloning and primary structure of the human blood group RhD polypeptide. Proc. Natl. Acad. Sci. USA 89, 10925-10929.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 10925-10929
-
-
Van Kim, C.L.1
Mouro, I.2
Cherif-Zahar, B.3
-
16
-
-
13244274799
-
Fetal genotyping
-
Hadley, A. G. and Soothill, P. W, eds, Cambridge University Press, Cambridge, UK
-
Avent, N. D. (2002) Fetal genotyping. In: Hadley, A. G. and Soothill, P. W. (eds.). Alloimmune disorders of pregnancy, pp 121-139. Cambridge University Press, Cambridge, UK.
-
(2002)
Alloimmune disorders of pregnancy
, pp. 121-139
-
-
Avent, N.D.1
-
17
-
-
17644444667
-
Prenatal determination of fetal blood group status
-
Avent, N. D., Finning, K. M., Martin, P. G., and Soothill, P. W. (2000) Prenatal determination of fetal blood group status. Vox Sang. 78, 155-162.
-
(2000)
Vox Sang
, vol.78
, pp. 155-162
-
-
Avent, N.D.1
Finning, K.M.2
Martin, P.G.3
Soothill, P.W.4
-
18
-
-
0031873052
-
Antenatal genotyping of the blood groups of the fetus
-
Avent, N. D. (1998) Antenatal genotyping of the blood groups of the fetus. Vox Sang. 74, 365-374.
-
(1998)
Vox Sang
, vol.74
, pp. 365-374
-
-
Avent, N.D.1
-
19
-
-
0023676666
-
Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains
-
Bloy, C., Blanchard, D., Dahr, W., Beyreuther, K., Salmon, C., and Cartron, J. P. (1988) Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains. Blood 72, 661-666.
-
(1988)
Blood
, vol.72
, pp. 661-666
-
-
Bloy, C.1
Blanchard, D.2
Dahr, W.3
Beyreuther, K.4
Salmon, C.5
Cartron, J.P.6
-
20
-
-
0024235956
-
Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane
-
Avent, N. D., Ridgwell, K., Wanner, M. J., and Anstee, D. J. (1988) Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane. Biochem. J. 256, 1043-1046.
-
(1988)
Biochem. J
, vol.256
, pp. 1043-1046
-
-
Avent, N.D.1
Ridgwell, K.2
Wanner, M.J.3
Anstee, D.J.4
-
21
-
-
0024024829
-
Polymorphism in the Mr 32,000 Rh protein purified from Rh(D)-positive and -negative erythrocytes
-
Saboori, A. M., Smith, B. L., and Agre, P. (1988) Polymorphism in the Mr 32,000 Rh protein purified from Rh(D)-positive and -negative erythrocytes. Proc. Natl. Acad. Sci. USA 85, 4042-4045.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4042-4045
-
-
Saboori, A.M.1
Smith, B.L.2
Agre, P.3
-
22
-
-
0027216648
-
Prenatal determination of fetal RhD type by DNA amplification
-
Bennett, P. R., Le Van Kim, C., Colin, Y., Warwick, R. M., Cherif-Zahar, R., Fisk, N. and 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
Le2
Van Kim, C.3
Colin, Y.4
Warwick, R.M.5
Cherif-Zahar, R.6
Fisk, N.7
Cartron, J.P.8
-
23
-
-
0025723965
-
Genetic basis of the RhD-positive and RhD-positive and RhD-negative blood group polymorphism as analysis
-
Colin, Y., Cherif-Zahar, F., Le Van Kim, C., Raynal, V., Van Huffel, V., and Cartron, J. P. (1991) Genetic basis of the RhD-positive and RhD-positive and RhD-negative blood group polymorphism as analysis. Blood 78, 2747-2752.
-
(1991)
Blood
, vol.78
, pp. 2747-2752
-
-
Colin, Y.1
Cherif-Zahar, F.2
Le3
Van Kim, C.4
Raynal, V.5
Van Huffel, V.6
Cartron, J.P.7
-
24
-
-
0026808712
-
Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression
-
Ridgwell, K., Spurr, N. K., Laguda, B., MacGeoch, C., Avent, N. D. and Tanner, M. J. (1992) Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression. Biochem. J. 287, 223-338.
-
(1992)
Biochem. J
, vol.287
, pp. 223-338
-
-
Ridgwell, K.1
Spurr, N.K.2
Laguda, B.3
MacGeoch, C.4
Avent, N.D.5
Tanner, M.J.6
-
25
-
-
0034659823
-
RHD gene deletion occurred in the Rhesus box
-
Wagner, F. F. and Flegel, W. A. (2000) RHD gene deletion occurred in the Rhesus box. Blood 95, 3662-3668.
-
(2000)
Blood
, vol.95
, pp. 3662-3668
-
-
Wagner, F.F.1
Flegel, W.A.2
-
26
-
-
15244354412
-
Genetic mechanisms of Rhesus box variation
-
Wagner, F. F., Moulds, J. M., and Flegel, W. A. (2005) Genetic mechanisms of Rhesus box variation. Transfusion 45, 338-344.
-
(2005)
Transfusion
, vol.45
, pp. 338-344
-
-
Wagner, F.F.1
Moulds, J.M.2
Flegel, W.A.3
-
27
-
-
0036560615
-
Novel 3′ Rhesus box sequences confound RHD zygosity assignment
-
Matheson, K. A. and Denomme, G. A. (2002) Novel 3′ Rhesus box sequences confound RHD zygosity assignment. Transfusion 42, 645-650.
-
(2002)
Transfusion
, vol.42
, pp. 645-650
-
-
Matheson, K.A.1
Denomme, G.A.2
-
28
-
-
0346243931
-
Current status of immunoprophylaxis with anti-D immunoglobin
-
Engelfriet, C. P., Reesink, H. W., Judd, W. J., et al. (2003) Current status of immunoprophylaxis with anti-D immunoglobin. Vox Sang. 85, 328-337.
-
(2003)
Vox Sang
, vol.85
, pp. 328-337
-
-
Engelfriet, C.P.1
Reesink, H.W.2
Judd, W.J.3
-
29
-
-
0031936115
-
-
Urbaniak, S. J. (1998) Consensus conference on anti-D prophylaxis, April 7 & 8, 1997: final consensus statement. Royal College of Physicians of Edinburgh/Royal College of Obstetricians and Gynaecologists. Transfusion. 38, 97-99.
-
Urbaniak, S. J. (1998) Consensus conference on anti-D prophylaxis, April 7 & 8, 1997: final consensus statement. Royal College of Physicians of Edinburgh/Royal College of Obstetricians and Gynaecologists. Transfusion. 38, 97-99.
-
-
-
-
30
-
-
33646068369
-
Non-invasive antenatal RHD typing
-
Van der Schoot, C. E., Soussan, A. A., Koelewijn, J., Bonsel, G., Paget-Christiaens, L. G., and de Haas, M. (2006) Non-invasive antenatal RHD typing. Transfus. Clin. Biol. 13, 53-57.
-
(2006)
Transfus. Clin. Biol
, vol.13
, pp. 53-57
-
-
Van der Schoot, C.E.1
Soussan, A.A.2
Koelewijn, J.3
Bonsel, G.4
Paget-Christiaens, L.G.5
de Haas, M.6
-
31
-
-
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. and Daniels, G. (2004) 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. 1022, 119-123.
-
(2004)
Ann. N Y Acad. Sci
, vol.1022
, pp. 119-123
-
-
Finning, K.1
Martin, P.2
Daniels, G.3
-
32
-
-
3342986296
-
Large-scale prediagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women
-
Rouillac-Le Sciellour, C., Puillandre, P., Gillot, R., et al. (2004) Large-scale prediagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women. Mol. Diagn. 8, 23-31.
-
(2004)
Mol. Diagn
, vol.8
, pp. 23-31
-
-
Rouillac-Le Sciellour, C.1
Puillandre, P.2
Gillot, R.3
-
33
-
-
14644422634
-
Fetal RhD genotyping by maternal serum analysis: A two-year experience
-
Gautier, E., Benachi, A., Giovangrand, Y., et al., (2005) Fetal RhD genotyping by maternal serum analysis: a two-year experience. Am. J. Obstet. Gynecol. 192, 666-669.
-
(2005)
Am. J. Obstet. Gynecol
, vol.192
, pp. 666-669
-
-
Gautier, E.1
Benachi, A.2
Giovangrand, Y.3
-
34
-
-
0024340286
-
Should anti-Rh immunoglobulin be given D variant women?
-
Lubenko, A., Contreras, M., and Habash, J. (1989) Should anti-Rh immunoglobulin be given D variant women? Br. J. Hematol. 72, 429-433.
-
(1989)
Br. J. Hematol
, vol.72
, pp. 429-433
-
-
Lubenko, A.1
Contreras, M.2
Habash, J.3
-
35
-
-
0020530949
-
Fatal hemolytic disease of a newborn due to anti-D in an Rh-positive Du variant mother
-
Lacey, P. A., Caskey, C. R., Werner, D. J., and Moulds, J. J. (1983) Fatal hemolytic disease of a newborn due to anti-D in an Rh-positive Du variant mother. Transfusion 23, 91-94.
-
(1983)
Transfusion
, vol.23
, pp. 91-94
-
-
Lacey, P.A.1
Caskey, C.R.2
Werner, D.J.3
Moulds, J.J.4
-
36
-
-
33646060398
-
Molecular genetics of RH and its clinical application Genetique moleculaire sur systeme RH et ses applications cliniques
-
Flegel, W. A. (2006) Molecular genetics of RH and its clinical application Genetique moleculaire sur systeme RH et ses applications cliniques. Transfus. Clin. Biol. 13, 4-12.
-
(2006)
Transfus. Clin. Biol
, vol.13
, pp. 4-12
-
-
Flegel, W.A.1
-
37
-
-
0034848225
-
Molecular biology of the Rh blood group system
-
Avent, N. D. (2001) Molecular biology of the Rh blood group system. J. Pediatr. Hematol. Oncol. 23, 394-402.
-
(2001)
J. Pediatr. Hematol. Oncol
, vol.23
, pp. 394-402
-
-
Avent, N.D.1
-
38
-
-
0032745701
-
The rhesus blood group system: Insights from recent advances in molecular biology
-
Avent, N. D. (1999) The rhesus blood group system: insights from recent advances in molecular biology. Transfus. Med. Rev. 13, 245-266.
-
(1999)
Transfus. Med. Rev
, vol.13
, pp. 245-266
-
-
Avent, N.D.1
-
39
-
-
3242701528
-
The structure and function of the molecules that carry human red blood cell and platelet antigens
-
Dénomme, G. A. (2004) The structure and function of the molecules that carry human red blood cell and platelet antigens. Transfus. Med. Rev. 18, 203-231.
-
(2004)
Transfus. Med. Rev
, vol.18
, pp. 203-231
-
-
Dénomme, G.A.1
-
40
-
-
0028322927
-
Prenatal determination of fetal RhD type
-
Simsek, S., Bleeker, P. M. and von dem Borne, A. E. (1994) Prenatal determination of fetal RhD type. N. Engl. J. Med. 330, 795-796.
-
(1994)
N. Engl. J. Med
, vol.330
, pp. 795-796
-
-
Simsek, S.1
Bleeker, P.M.2
von dem3
Borne, A.E.4
-
41
-
-
0028290884
-
Prenatal determination of fetal RhD type
-
Carritt, B., Steers, F. J., and Avent, N. D. (1994) Prenatal determination of fetal RhD type. Lancet 344, 205-206.
-
(1994)
Lancet
, vol.344
, pp. 205-206
-
-
Carritt, B.1
Steers, F.J.2
Avent, N.D.3
-
42
-
-
0030945033
-
Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene
-
Avent, N. D., Martin, P. G., Armstrong-Fisher, S. S., et al. (1997) Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood 89, 2568-2577.
-
(1997)
Blood
, vol.89
, pp. 2568-2577
-
-
Avent, N.D.1
Martin, P.G.2
Armstrong-Fisher, S.S.3
-
43
-
-
0032170573
-
The RhD-trait in a white patient with the RhCCee phenotype attributed to a four-nucleotide deletion in the RHD gene
-
Andrews, K. T., Wolter, L. C., Saul, A., and Hyland, C. A. (1998) The RhD-trait in a white patient with the RhCCee phenotype attributed to a four-nucleotide deletion in the RHD gene. Blood 92, 1839-1840.
-
(1998)
Blood
, vol.92
, pp. 1839-1840
-
-
Andrews, K.T.1
Wolter, L.C.2
Saul, A.3
Hyland, C.A.4
-
44
-
-
0029815713
-
Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: Phenotypic homozygosity versus genotypic heterozygosity
-
Huang, C. H. (1996) Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: phenotypic homozygosity versus genotypic heterozygosity. Blood 88, 2326-2333.
-
(1996)
Blood
, vol.88
, pp. 2326-2333
-
-
Huang, C.H.1
-
45
-
-
18744410167
-
RHD positive haplotypes in D negative Europeans
-
Wagner, F. F., Frohmajer, A., and Flegel, W. A. (2001) RHD positive haplotypes in D negative Europeans. BMC Genet. 2, 10.
-
(2001)
BMC Genet
, vol.2
, pp. 10
-
-
Wagner, F.F.1
Frohmajer, A.2
Flegel, W.A.3
-
46
-
-
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, B. K., Green, C. A., Avent, N. D., et al. (2000) 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 95, 12-18.
-
(2000)
Blood
, vol.95
, pp. 12-18
-
-
Singleton, B.K.1
Green, C.A.2
Avent, N.D.3
-
47
-
-
0031671377
-
The VS and V blood group polymorphisms in Africans: A serologic and molecular analysis
-
Daniels, G. L., Faas, B. H., Green, C. A., et al. (1998) The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion. 38, 951-958.
-
(1998)
Transfusion
, vol.38
, pp. 951-958
-
-
Daniels, G.L.1
Faas, B.H.2
Green, C.A.3
-
48
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas, B. H., et al. (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.1
-
49
-
-
0036692036
-
Prediction of fetal D status from maternal plasma: Introduction of a new noninvasive fetal RHD genotyping service
-
Finning, K. M., Martin, P. G., Soothill, P. W., and Avent, N. D. (2002) Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service. Transfusion 42, 1079-1085.
-
(2002)
Transfusion
, vol.42
, pp. 1079-1085
-
-
Finning, K.M.1
Martin, P.G.2
Soothill, P.W.3
Avent, N.D.4
-
50
-
-
0029827480
-
Quantitation of Rh D antigen sites on weak D and D variant red cells by flow cytometry
-
Jones, J. W., Lloyd-Evans, P., and Kumpel, B. M. (1996) Quantitation of Rh D antigen sites on weak D and D variant red cells by flow cytometry. Vox Sang. 71, 176-183.
-
(1996)
Vox Sang
, vol.71
, pp. 176-183
-
-
Jones, J.W.1
Lloyd-Evans, P.2
Kumpel, B.M.3
-
51
-
-
0032521490
-
Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features
-
Wagner, F. F., Gassner, C., Muller, T. H., Schonitzer, D., Schunter, F., and Flegel, W. A. (1998) Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Blood 91, 2157-2168.
-
(1998)
Blood
, vol.91
, pp. 2157-2168
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
Schonitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
52
-
-
0025689034
-
Rh immunization by the partial D antigen of category DVa
-
Mayne, K., Bowell, P., Woodward, T., Sibley, C., Lomas, C., and Tippett, P. (1990) Rh immunization by the partial D antigen of category DVa. Br. J. Haematol. 76, 537-539.
-
(1990)
Br. J. Haematol
, vol.76
, pp. 537-539
-
-
Mayne, K.1
Bowell, P.2
Woodward, T.3
Sibley, C.4
Lomas, C.5
Tippett, P.6
-
53
-
-
0027373056
-
Severe hemolytic disease of the newborn caused by anti-Gonzales antibody
-
Leschek, E., Pearlman, S. A., Boudreaux, I., and Meek, R. (1993) Severe hemolytic disease of the newborn caused by anti-Gonzales antibody. Am. J. Perinatol. 10, 362-364.
-
(1993)
Am. J. Perinatol
, vol.10
, pp. 362-364
-
-
Leschek, E.1
Pearlman, S.A.2
Boudreaux, I.3
Meek, R.4
-
54
-
-
0021049532
-
The Rh antigen Tar (Rh40) causing haemolytic disease of the newborn
-
Levene, C., Sela, R., Grunberg, L., Gale, R., Lomas, C., and Tippett, P. (1983) The Rh antigen Tar (Rh40) causing haemolytic disease of the newborn. Clin. Lab. Haematol. 5, 303-305.
-
(1983)
Clin. Lab. Haematol
, vol.5
, pp. 303-305
-
-
Levene, C.1
Sela, R.2
Grunberg, L.3
Gale, R.4
Lomas, C.5
Tippett, P.6
-
55
-
-
0023639306
-
Anti-Rh 29 in a primigrávida with rhesus null syndrome resulting in haemolytic disease of the newborn
-
Gabra, G. S., Bruce, M., Watt, A., and Mitchell, R. (1987) Anti-Rh 29 in a primigrávida with rhesus null syndrome resulting in haemolytic disease of the newborn. Vox Sang. 53, 143-146.
-
(1987)
Vox Sang
, vol.53
, pp. 143-146
-
-
Gabra, G.S.1
Bruce, M.2
Watt, A.3
Mitchell, R.4
-
56
-
-
0033863272
-
Moderate hemolytic disease of the newborn due to anti-HrO in a mother with the D-/D- phenotype
-
Lenkiewicz, B. and Zupanska, B. (2000) Moderate hemolytic disease of the newborn due to anti-HrO in a mother with the D-/D- phenotype. Immunohematology 16, 109-111.
-
(2000)
Immunohematology
, vol.16
, pp. 109-111
-
-
Lenkiewicz, B.1
Zupanska, B.2
-
57
-
-
0026671549
-
Severe haemolytic disease in an infant born to an Rh(null) proposita
-
Lubenko, A., Contreras, M., Portugal, C. L., et al. (1992) Severe haemolytic disease in an infant born to an Rh(null) proposita. Vox Sang. 63, 43-47.
-
(1992)
Vox Sang
, vol.63
, pp. 43-47
-
-
Lubenko, A.1
Contreras, M.2
Portugal, C.L.3
-
58
-
-
24144490009
-
Optimized real-time quantitative PCR measurement of male fetal DNA in maternal plasma
-
Zimmermann, B., El-Sheikhah, A., Nicolaides, K., Holzgreve, W., and Hahn, S. (2005) Optimized real-time quantitative PCR measurement of male fetal DNA in maternal plasma. Clin. Chem. 51, 1598-1604.
-
(2005)
Clin. Chem
, vol.51
, pp. 1598-1604
-
-
Zimmermann, B.1
El-Sheikhah, A.2
Nicolaides, K.3
Holzgreve, W.4
Hahn, S.5
-
59
-
-
14944360372
-
Report of the First International Workshop on molecular blood group genotyping
-
Daniels, G., van der Schoot, C. E., and Olsson, M. L. (2005) Report of the First International Workshop on molecular blood group genotyping. Vox Sang. 88, 136-142.
-
(2005)
Vox Sang
, vol.88
, pp. 136-142
-
-
Daniels, G.1
van der Schoot, C.E.2
Olsson, M.L.3
-
60
-
-
0037097590
-
Quantitative assessment of hematopoietic chimerism after bone marrow transplantation by real-time quantitative polymerase chain reaction
-
Alizadeh, M., Bernard, M., Danic, B., et al. (2002) Quantitative assessment of hematopoietic chimerism after bone marrow transplantation by real-time quantitative polymerase chain reaction. Blood 99, 4618-4625.
-
(2002)
Blood
, vol.99
, pp. 4618-4625
-
-
Alizadeh, M.1
Bernard, M.2
Danic, B.3
-
61
-
-
26844478953
-
Detection of the placental epigenetic signature of the maspin gene in maternal plasma
-
Chim, S. S., Tong, Y. K., Chiu, R. W., et al. (2005) Detection of the placental epigenetic signature of the maspin gene in maternal plasma. Proc. Natl. Acad. Sci. USA 102, 14753-14758.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 14753-14758
-
-
Chim, S.S.1
Tong, Y.K.2
Chiu, R.W.3
-
62
-
-
33845512998
-
Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis
-
Chang, et al., (2006) Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem. 52, 2211-2218.
-
(2006)
Clin Chem
, vol.52
, pp. 2211-2218
-
-
Chang1
-
63
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo, Y. M., Corbetta, N., Chamberlain, P. F., et al. (1997) Presence of fetal DNA in maternal plasma and serum. Lancet 350, 485-487.
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
-
64
-
-
34548757303
-
Workshop report on the extraction of foetal DNA from maternal plasma
-
Legier, et al. (2007) Workshop report on the extraction of foetal DNA from maternal plasma. Prenatal Diagnosis 27, 824-829.
-
(2007)
Prenatal Diagnosis
, vol.27
, pp. 824-829
-
-
Legier1
-
65
-
-
85069134998
-
Rapid molecular genotyping for RHD using multiplex ligation-dependent probe amplification technology
-
Madgett, T. E. (2005) Rapid molecular genotyping for RHD using multiplex ligation-dependent probe amplification technology. Transfusion 45, 129A.
-
(2005)
Transfusion
, vol.45
-
-
Madgett, T.E.1
-
66
-
-
1642574222
-
Size distributions of maternal and fetal DNA in maternal plasma
-
Chan, K. C., Zhang, J., Hui, A. B., et al. (2004) Size distributions of maternal and fetal DNA in maternal plasma. Clin. Chem. 50, 88-92.
-
(2004)
Clin. Chem
, vol.50
, pp. 88-92
-
-
Chan, K.C.1
Zhang, J.2
Hui, A.B.3
-
67
-
-
13844269123
-
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma
-
Li, Y., Di Naro, E., Vitucci, A., Zimmermann, B., Holzgreve, W., and Hahn, S. (2005) Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. J. Am. Med. Assoc. 293, 843-849.
-
(2005)
J. Am. Med. Assoc
, vol.293
, pp. 843-849
-
-
Li, Y.1
Di Naro, E.2
Vitucci, A.3
Zimmermann, B.4
Holzgreve, W.5
Hahn, S.6
-
68
-
-
20144388742
-
Presence of RHD in serologically D-, C/E+ individuals: A European multicenter study
-
Gassner, C., Doescher, A., Drnovsek, T. D., et al. (2005) Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study. Transfusion. 45, 527-538.
-
(2005)
Transfusion
, vol.45
, pp. 527-538
-
-
Gassner, C.1
Doescher, A.2
Drnovsek, T.D.3
-
69
-
-
2442477666
-
A new hybrid RHD-positive, D antigen-negative allele
-
Shao, C. P. and Xiong, W. (2004) A new hybrid RHD-positive, D antigen-negative allele. Transfus. Med. 14, 185-186.
-
(2004)
Transfus. Med
, vol.14
, pp. 185-186
-
-
Shao, C.P.1
Xiong, W.2
-
70
-
-
0027993037
-
Serotype switching in a partially deleted RHD gene
-
Blunt, T., Daniels, G., and 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
-
71
-
-
0030017665
-
Involvement of Ser103 of the Rh polypeptides in G epitope formation
-
Faas, B. H., Beckers, E. A., Simsek, S., et al. (1996) Involvement of Ser103 of the Rh polypeptides in G epitope formation. Transfusion 36, 506-11.
-
(1996)
Transfusion
, vol.36
, pp. 506-511
-
-
Faas, B.H.1
Beckers, E.A.2
Simsek, S.3
-
72
-
-
0030838226
-
RHD/CE typing by polymerase chain reaction using sequence-specific primers
-
Gassner, C., Schmarda A., Kilga-Nogler, S., et al. (1997) RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 37, 1020-1026.
-
(1997)
Transfusion
, vol.37
, pp. 1020-1026
-
-
Gassner, C.1
Schmarda, A.2
Kilga-Nogler, S.3
-
73
-
-
0012514010
-
Molecular background of Rh D-positive, D-negative, D(el), and weak D phenotypes in Chinese
-
Shao, C. P., Maas, J. H., Su, Y. Q., Kohler, M., and Legler, T. J. (2002) Molecular background of Rh D-positive, D-negative, D(el), and weak D phenotypes in Chinese. Vox Sang. 83, 156-161.
-
(2002)
Vox Sang
, vol.83
, pp. 156-161
-
-
Shao, C.P.1
Maas, J.H.2
Su, Y.Q.3
Kohler, M.4
Legler, T.J.5
-
74
-
-
7344259638
-
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemia
-
Cherif-Zahar, B., Bony, V., Steffensen, R., et al. (1998) Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemia. Br. J. Haematol. 102, 1263-1270.
-
(1998)
Br. J. Haematol
, vol.102
, pp. 1263-1270
-
-
Cherif-Zahar, B.1
Bony, V.2
Steffensen, R.3
-
75
-
-
0030742588
-
The RHD gene is highly detectable in RhD-negative Japanese donors
-
Okuda, H., Kawano, M., Iwamoto, S., et al. (1997) The RHD gene is highly detectable in RhD-negative Japanese donors. J. Clin. Invest. 100, 373-379.
-
(1997)
J. Clin. Invest
, vol.100
, pp. 373-379
-
-
Okuda, H.1
Kawano, M.2
Iwamoto, S.3
-
76
-
-
13444265943
-
Systemic analysis and zygosity determination of the RHD gene in a D-negative Chinese Han population reveals a novel D-negative RHD gene
-
Qun, X., Grootkerk-Tax, M. G., Maaskant-van Wijk, P. A., and van der Schoot, C. E. (2005) 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. 88, 35-40.
-
(2005)
Vox Sang
, vol.88
, pp. 35-40
-
-
Qun, X.1
Grootkerk-Tax, M.G.2
Maaskant-van Wijk, P.A.3
van der Schoot, C.E.4
-
77
-
-
15244361715
-
Molecular characterization of D- Korean persons: Development of a diagnostic strategy
-
Kim, J. Y., Kim, S. Y., Kim, C. A., Yon, G. S., and Park, S. S. (2005) Molecular characterization of D- Korean persons: development of a diagnostic strategy. Transfusion 45, 345-352.
-
(2005)
Transfusion
, vol.45
, pp. 345-352
-
-
Kim, J.Y.1
Kim, S.Y.2
Kim, C.A.3
Yon, G.S.4
Park, S.S.5
-
78
-
-
0032505654
-
Detection of fetal RHD-specific sequences in maternal plasma
-
1196
-
Faas, B. H., Beuling, E. A., Christiaens, G. C., von dem Borne, A. E., and van der Schoot, C. E. (1998) Detection of fetal RHD-specific sequences in maternal plasma. Lancet 352, 1196.
-
(1998)
Lancet
, vol.352
-
-
Faas, B.H.1
Beuling, E.A.2
Christiaens, G.C.3
von dem4
Borne, A.E.5
van der6
Schoot, C.E.7
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