-
1
-
-
0027216648
-
Prenatal determination of fetal RhD type by DNA amplification
-
Bennett PR, Le Van Kim C, Colin Y, Warwick RM, et al. (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
-
2
-
-
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, VanAgtmael AL, et al. (2011). Fetal RHD genotype detection from circulating cell-free fetal DNA in maternal plasma in non-sensitized RhD negative women. Prenat. Diagn. 31: 802-808.
-
(2011)
Prenat. Diagn
, vol.31
, pp. 802-808
-
-
Bombard, A.T.1
Akolekar, R.2
Farkas, D.H.3
VanAgtmael, A.L.4
-
3
-
-
3242760515
-
RHD 1227A is an important genetic marker for RhD(el) individuals
-
Chen JC, Lin TM, Chen YL, Wang YH, et al. (2004). RHD 1227A is an important genetic marker for RhD(el) individuals. Am. J. Clin. Pathol. 122: 193-198.
-
(2004)
Am. J. Clin. Pathol
, vol.122
, pp. 193-198
-
-
Chen, J.C.1
Lin, T.M.2
Chen, Y.L.3
Wang, Y.H.4
-
4
-
-
77958113868
-
Noninvasive determination of fetal rh blood group, D antigen status by cell-free DNA analysis in maternal plasma: Experience in a Brazilian population
-
Chinen PA, Nardozza LM, Martinhago CD, Camano L, et al. (2010). Noninvasive determination of fetal rh blood group, D antigen status by cell-free DNA analysis in maternal plasma: experience in a Brazilian population. Am. J. Perinatol. 27: 759-762.
-
(2010)
Am. J. Perinatol
, vol.27
, pp. 759-762
-
-
Chinen, P.A.1
Nardozza, L.M.2
Martinhago, C.D.3
Camano, L.4
-
5
-
-
34249826320
-
Report of the second international workshop on molecular blood group genotyping
-
Daniels G, van der Schoot CE and Olsson ML (2007). Report of the second international workshop on molecular blood group genotyping. Vox Sang. 93: 83-88.
-
(2007)
Vox Sang
, vol.93
, pp. 83-88
-
-
Daniels, G.1
van der Schoot, C.E.2
Olsson, M.L.3
-
6
-
-
59649114083
-
Noninvasive prenatal diagnosis of fetal blood group phenotypes: Current practice and future prospects
-
Daniels G, Finning K, Martin P and Massey E (2009). Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects. Prenat. Diagn. 29: 101-107.
-
(2009)
Prenat. Diagn
, vol.29
, pp. 101-107
-
-
Daniels, G.1
Finning, K.2
Martin, P.3
Massey, E.4
-
7
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas BHW, Beckers EAM, Wildoer P, Lightart PC, 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.W.1
Beckers, E.A.M.2
Wildoer, P.3
Lightart, P.C.4
-
8
-
-
0031953137
-
The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease
-
Huang CH (1998). The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease. J. Biol. Chem. 273: 2207-2213.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 2207-2213
-
-
Huang, C.H.1
-
9
-
-
0036628978
-
Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype
-
Rodrigues A, Rios M, Pellegrino J Jr, Costa FF, et al. (2002). Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype. Braz. J. Med. Biol. Res. 35: 767-773.
-
(2002)
Braz. J. Med. Biol. Res
, vol.35
, pp. 767-773
-
-
Rodrigues, A.1
Rios, M.2
Pellegrino, J.3
Costa, F.F.4
-
10
-
-
3342986296
-
Large-scale pre-diagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women
-
Rouillac-Le SC, Puillandre P, Gillot R, Baulard C, et al. (2004). Large-scale pre-diagnosis 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, S.C.1
Puillandre, P.2
Gillot, R.3
Baulard, C.4
-
11
-
-
42949094614
-
Noninvasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD
-
Rouillac-Le SC, Serazin V, Brossard Y, Oudin O, et al. (2007). Noninvasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD. Transfus. Clin. Biol. 14: 572-577.
-
(2007)
Transfus. Clin. Biol
, vol.14
, pp. 572-577
-
-
Rouillac-Le, S.C.1
Serazin, V.2
Brossard, Y.3
Oudin, O.4
-
12
-
-
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 and de Haas M (2011). 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 118: 1340-1348.
-
(2011)
BJOG
, vol.118
, pp. 1340-1348
-
-
Scheffer, P.1
van der Schoot, C.2
Page-Christiaens, G.3
de Haas, M.4
-
13
-
-
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, Martin PG, 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
Martin, P.G.4
-
14
-
-
0034659823
-
RHD gene deletion occurred in the Rhesus box
-
Wagner FF and Flegel WA (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
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