-
1
-
-
48549093650
-
Management of rhesus alloimmunization in pregnancy
-
76. Review.
-
Moise KJ Jr. Management of rhesus alloimmunization in pregnancy. Obstet Gynecol 2008;112:164-76. Review.
-
(2008)
Obstet Gynecol
, vol.112
, pp. 164
-
-
Moise Jr., K.J.1
-
2
-
-
84873243364
-
-
Routine antenatal anti-D prophylaxis for women who are rhesus D negative. Review of NICE technology appraisal guidance 41. National Institute for Clinical Excellence.
-
Routine antenatal anti-D prophylaxis for women who are rhesus D negative. Review of NICE technology appraisal guidance 41. National Institute for Clinical Excellence.
-
-
-
-
3
-
-
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. 3662-3668
-
-
Wagner, F.F.1
Flegel, W.A.2
-
4
-
-
0025723965
-
Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis
-
Colin Y, Chérif-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
Chérif-Zahar, B.2
Le Van Kim, C.3
-
5
-
-
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
-
6
-
-
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
-
7
-
-
0031671377
-
The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis
-
Daniels GL, Faas BH, Green CA, et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion 1998;38:951-8.
-
(1998)
Transfusion
, vol.38
, pp. 951-958
-
-
Daniels, G.L.1
Faas, B.H.2
Green, C.A.3
-
8
-
-
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
-
9
-
-
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
-
10
-
-
0032505654
-
Detection of fetal RHD-specific sequences in maternal plasma
-
Faas BH, Beuling EA, Christiaens GC, et al. Detection of fetal RHD-specific sequences in maternal plasma. Lancet 1998;352:1196.
-
(1998)
Lancet
, vol.352
, pp. 1196
-
-
Faas, B.H.1
Beuling, E.A.2
Christiaens, G.C.3
-
11
-
-
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. 1079-1085
-
-
Finning, K.M.1
Martin, P.G.2
Soothill, P.W.3
Avent, N.D.4
-
12
-
-
55349105463
-
The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible
-
Müller SP, Bartels I, Stein W, et al. The determination of the fetal D status from maternal plasma for decision making on Rh prophylaxis is feasible. Transfusion 2008;48:2292-301.
-
(2008)
Transfusion
, vol.48
, pp. 2292-2301
-
-
Müller, S.P.1
Bartels, I.2
Stein, W.3
-
13
-
-
42949094614
-
Noninvasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD
-
7.
-
Rouillac-Le Sciellour C, Sérazin V, Brossard Y, et al. Noninvasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD. Transfus Clin Biol 2007;14:572-7.
-
(2007)
Transfus Clin Biol
, vol.14
, pp. 572
-
-
Rouillac-Le Sciellour, C.1
Sérazin, V.2
Brossard, Y.3
-
14
-
-
38349175325
-
Routine fetal RHD genotyping with maternal plasma: a four-year experience in Belgium
-
Minon JM, Gerard C, Senterre JM, et al. Routine fetal RHD genotyping with maternal plasma: a four-year experience in Belgium. Transfusion 2008;48:373-81.
-
(2008)
Transfusion
, vol.48
, pp. 373-381
-
-
Minon, J.M.1
Gerard, C.2
Senterre, J.M.3
-
15
-
-
0036402416
-
Fetal RHD genotyping in maternal serum during the first trimester of pregnancy
-
Costa JM, Giovangrandi Y, Ernault P, et al. Fetal RHD genotyping in maternal serum during the first trimester of pregnancy. Br J Haematol 2002;119:255-60.
-
(2002)
Br J Haematol
, vol.119
, pp. 255-260
-
-
Costa, J.M.1
Giovangrandi, Y.2
Ernault, P.3
-
16
-
-
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
-
17
-
-
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
-
18
-
-
79959314844
-
Fetal RHD genotyping in maternal plasma at 11-13 weeks of gestation
-
Akolekar R, Finning K, Kuppusamy R, et al. Fetal RHD genotyping in maternal plasma at 11-13 weeks of gestation. Fetal Diagn Ther 2011;29:301-6.
-
(2011)
Fetal Diagn Ther
, vol.29
, pp. 301-306
-
-
Akolekar, R.1
Finning, K.2
Kuppusamy, R.3
-
19
-
-
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
-
20
-
-
79960564291
-
Fetal RHD genotype detection from circulating cell-free fetal DNA in maternal plasma in non-sensitized RhD negative women
-
Bombard AT, Akolekar R, Farkas DH, et al. Fetal RHD genotype detection from circulating cell-free fetal DNA in maternal plasma in non-sensitized RhD negative women. Prenat Diagn 2011;31:802-8.
-
(2011)
Prenat Diagn
, vol.31
, pp. 802-808
-
-
Bombard, A.T.1
Akolekar, R.2
Farkas, D.H.3
-
21
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis
-
Lo YMD, Tein MSC, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet 1998;62:768-75.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 768-775
-
-
Lo, Y.M.D.1
Tein, M.S.C.2
Lau, T.K.3
-
22
-
-
77957364707
-
Fetal sex determination using circulating cell-free fetal DNA (ccffDNA) at 11 to 13 weeks of gestation
-
Akolekar R, Farkas DH, VanAgtmael AL, et al. Fetal sex determination using circulating cell-free fetal DNA (ccffDNA) at 11 to 13 weeks of gestation. Prenat Diagn 2010;30:918-23.
-
(2010)
Prenat Diagn
, vol.30
, pp. 918-923
-
-
Akolekar, R.1
Farkas, D.H.2
VanAgtmael, A.L.3
-
23
-
-
33845512998
-
Hypermethylated RASSF1A in maternal plasma: a universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis
-
Chan KC, Ding C, Gerovassili A, et al. Hypermethylated RASSF1A in maternal plasma: a universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem 2006;52:2211-8.
-
(2006)
Clin Chem
, vol.52
, pp. 2211-2218
-
-
Chan, K.C.1
Ding, C.2
Gerovassili, A.3
-
24
-
-
80054071226
-
Restriction enzyme-mediated enhanced detection of circulating cell-free fetal DNA in maternal plasma
-
Tynan JA, Mahboubi P, Cagasan LL, et al. Restriction enzyme-mediated enhanced detection of circulating cell-free fetal DNA in maternal plasma. J Mol Diagn 2011;13:382-9.
-
(2011)
J Mol Diagn
, vol.13
, pp. 382-389
-
-
Tynan, J.A.1
Mahboubi, P.2
Cagasan, L.L.3
-
26
-
-
33645304041
-
The D category VI type 4 allele is prevalent in the Spanish population
-
Esteban R, Montero R, Flegel WA, et al. The D category VI type 4 allele is prevalent in the Spanish population. Transfusion 2006;46:616-23.
-
(2006)
Transfusion
, vol.46
, pp. 616-623
-
-
Esteban, R.1
Montero, R.2
Flegel, W.A.3
-
27
-
-
3342986296
-
Large-scale pre-diagnosis 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. 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.
-
(2004)
Mol Diagn
, vol.8
, pp. 23-31
-
-
Rouillac-Le Sciellour, C.1
Puillandre, P.2
Gillot, R.3
-
29
-
-
84864247102
-
Rh immunoprophylaxis and fetal RHD genotyping: where are we going?
-
Queenan JT. Rh immunoprophylaxis and fetal RHD genotyping: where are we going? Obstet Gynecol 2012;120:219-20.
-
(2012)
Obstet Gynecol
, vol.120
, pp. 219-220
-
-
Queenan, J.T.1
|