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Volumn 29, Issue 4, 2011, Pages 301-306

Fetal RHD genotyping in maternal plasma at 11-13 weeks of gestation

Author keywords

Cell free fetal DNA; Fetal RHD genotyping; First trimester; Pyramid of prenatal care

Indexed keywords

CIRCULATING CELL FREE FETAL DNA; DNA; RHESUS D ANTIGEN; UNCLASSIFIED DRUG;

EID: 79959314844     PISSN: 10153837     EISSN: 14219964     Source Type: Journal    
DOI: 10.1159/000322959     Document Type: Article
Times cited : (44)

References (28)
  • 4
    • 0036692036 scopus 로고    scopus 로고
    • 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 42:1079-1085.
    • (2002) Transfusion , vol.42 , pp. 1079-1085
    • Finning, K.M.1    Martin, P.G.2    Soothill, P.W.3    Avent, N.D.4
  • 5
    • 0023197069 scopus 로고
    • Feto-maternal haemorrhage associated with genetic amniocentesis: Results of a randomized trial
    • Tabor A, Bang J, Nørgaard-Pedersen B: Fetomaternal haemorrhage associated with genetic amniocentesis: results of a randomized trial. Br J Obstet Gynaecol 1987;94:528-534. (Pubitemid 17077761)
    • (1987) British Journal of Obstetrics and Gynaecology , vol.94 , Issue.6 , pp. 528-534
    • Tabor, A.1    Bang, J.2    Norgaard-Pedersen, B.3
  • 6
    • 0022612562 scopus 로고
    • Feto-maternal transfusion after chorionic villus sampling: Clinical implications
    • Brambati B, Guercilena S, Bonacchi I, Oldrini A, Lanzani A, Piceni L: Feto-maternal transfusion after chorionic villus sampling: clinical implications. Hum Reprod 1986;1:37-40. (Pubitemid 16112429)
    • (1986) Human Reproduction , vol.1 , Issue.1 , pp. 37-40
    • Brambati, B.1    Guercilena, S.2    Bonacchi, I.3
  • 7
    • 33748787168 scopus 로고    scopus 로고
    • Diagnostic accuracy of noninvasive fetal Rh genotyping from maternal blood-A meta-analysis
    • DOI 10.1016/j.ajog.2006.07.033, PII S0002937806009641
    • 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: 1163-1173. (Pubitemid 44415679)
    • (2006) American Journal of Obstetrics and Gynecology , vol.195 , Issue.4 , pp. 1163-1173
    • Geifman-Holtzman, O.1    Grotegut, C.A.2    Gaughan, J.P.3
  • 9
    • 59649114083 scopus 로고    scopus 로고
    • Noninvasive prenatal diagnosis of fetal blood group phenotypes: Current practice and future prospects
    • Daniels G, Finning K, Martin P, Massey E: Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects. Prenat Diagn 2009;29:101-107.
    • (2009) Prenat Diagn , vol.29 , pp. 101-107
    • Daniels, G.1    Finning, K.2    Martin, P.3    Massey, E.4
  • 11
    • 42249108710 scopus 로고    scopus 로고
    • 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
    • DOI 10.1136/bmj.39518.463206.25
    • Finning K, Martin P, Summers J, Massey E, Poole G, Daniels G: 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;336:816-818. (Pubitemid 351548224)
    • (2008) BMJ , vol.336 , Issue.7648 , pp. 816-818
    • Finning, K.1    Martin, P.2    Summers, J.3    Massey, E.4    Poole, G.5    Daniels, G.6
  • 12
    • 0032146382 scopus 로고    scopus 로고
    • UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation
    • DOI 10.1016/S0140-6736(97)11280-6
    • Snijders RJ, Noble P, Sebire N, Souka A, Nicolaides KH: UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Lancet 1998;352:343-346. (Pubitemid 28352196)
    • (1998) Lancet , vol.352 , Issue.9125 , pp. 343-346
    • Snijders, R.J.M.1    Noble, P.2    Sebire, N.3    Souka, A.4    Nicolaides, K.H.5
  • 13
    • 51949091028 scopus 로고    scopus 로고
    • Screening for trisomy 21 by maternal age, fetal nuchal translucency thickness, free β-human chorionic gonadotropin, and pregnancy-associated plasma protein-A
    • Kagan KO, Wright D, Baker A, Sahota D, Nicolaides KH: Screening for trisomy 21 by maternal age, fetal nuchal translucency thickness, free β-human chorionic gonadotropin, and pregnancy-associated plasma protein-A. Ultrasound Obstet Gynecol 2008;31:618-624.
    • (2008) Ultrasound Obstet Gynecol , vol.31 , pp. 618-624
    • Kagan, K.O.1    Wright, D.2    Baker, A.3    Sahota, D.4    Nicolaides, K.H.5
  • 14
    • 0030035550 scopus 로고    scopus 로고
    • Molecular cloning and functional characterization of a novel human CC chemokine receptor (CCR5) for RANTES, MIP-1β, and MIP-1α
    • DOI 10.1074/jbc.271.29.17161
    • Raport CJ, Gosling J, Schweickart VL, Gray PW, Charo IF: Molecular cloning and functional characterization of a novel human CC chemokine receptor (CCR5) for RANTES, MIP-1β, and MIP-1α. J Biol Chem 1996;271:17161-17166. (Pubitemid 26244268)
    • (1996) Journal of Biological Chemistry , vol.271 , Issue.29 , pp. 17161-17166
    • Raport, C.J.1    Gosling, J.2    Schweickart, V.L.3    Gray, P.W.4    Charo, I.F.5
  • 17
    • 0347504842 scopus 로고    scopus 로고
    • Prenatal genotyping of RHD and SRY using maternal blood
    • DOI 10.1111/j.0042-9007.2003.00371.x
    • Randen I, Hauge R, Kjeldsen-Kragh J, Fagerhol MK: Prenatal genotyping of RHD and SRY using maternal blood. Vox Sang 2003; 85: 300-306. (Pubitemid 37522604)
    • (2003) Vox Sanguinis , vol.85 , Issue.4 , pp. 300-306
    • Randen, I.1    Hauge, R.2    Kjeldsen-Kragh, J.3    Fagerhol, M.K.4
  • 18
    • 26944483571 scopus 로고    scopus 로고
    • Noninvasive determination of fetal RHD status by examination of cell-free DNA in maternal plasma
    • DOI 10.1111/j.1537-2995.2005.00559.x
    • 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: 1473-1480. (Pubitemid 44194651)
    • (2005) Transfusion , vol.45 , Issue.9 , pp. 1473-1480
    • Brojer, E.1    Iupanska, B.2    Guz, K.3    Orzinska, A.4    Kalinska, A.5
  • 19
    • 34548106343 scopus 로고    scopus 로고
    • Polymerase-chain-reaction-based detection of fetal rhesus D and Y-chromosome-specific DNA in the whole blood of pregnant women during different trimesters of pregnancy
    • DOI 10.1159/000104803
    • Al-Yatama MK, Mustafa AS, Al-Kandari FM, Khaja N, Zohra K, Monem RA, Abraham S: Polymerase-chain-reaction-based detection of fetal rhesus D and Y-chromosome-specific DNA in the whole blood of pregnant women during different trimesters of pregnancy. Med Princ Pract 2007;16:327-332. (Pubitemid 47294486)
    • (2007) Medical Principles and Practice , vol.16 , Issue.5 , pp. 327-332
    • Al-Yatama, M.K.1    Mustafa, A.S.2    Al-Kandari, F.M.3    Khaja, N.4    Zohra, K.5    Monem, R.A.6    Abraham, S.7
  • 21
    • 38349175325 scopus 로고    scopus 로고
    • Routine fetal RHD genotyping with maternal plasma: A four-year experience in Belgium
    • Minon JM, Gerard C, Senterre JM, Schaaps JP, Foidart JM: Routine fetal RHD genotyping with maternal plasma: a four-year experience in Belgium. Transfusion 2008;48:373-381.
    • (2008) Transfusion , vol.48 , pp. 373-381
    • Minon, J.M.1    Gerard, C.2    Senterre, J.M.3    Schaaps, J.P.4    Foidart, J.M.5
  • 22
    • 0033957696 scopus 로고    scopus 로고
    • 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, Smart E, Daka A, Narter-Olaga EG, Hawthorne LM, Daniels G: 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;95:12-18. (Pubitemid 30017219)
    • (2000) Blood , vol.95 , Issue.1 , pp. 12-18
    • Singleton, B.K.1    Green, C.A.2    Avent, N.D.3    Martin, P.G.4    Smart, E.5    Daka, A.6    Narter-Olaga, E.G.7    Hawthorne, L.M.8    Daniels, G.9
  • 23
    • 59249101943 scopus 로고    scopus 로고
    • Noninvasive fetal RHD genotyping tests: A systematic review of the quality of reporting of diagnostic accuracy in published studies
    • Freeman K, Szczepura A, Osipenko L: Noninvasive fetal RHD genotyping tests: a systematic review of the quality of reporting of diagnostic accuracy in published studies. Eur J Obstet Gynecol Reprod Biol 2009;142:91-98.
    • (2009) Eur J Obstet Gynecol Reprod Biol , vol.142 , pp. 91-98
    • Freeman, K.1    Szczepura, A.2    Osipenko, L.3
  • 24
    • 58049202879 scopus 로고    scopus 로고
    • The use of cell-free fetal nucleic acids in maternal blood for noninvasive prenatal diagnosis
    • Wright CF, Burton H: The use of cell-free fetal nucleic acids in maternal blood for noninvasive prenatal diagnosis. Hum Reprod Update 2009;15:139-151.
    • (2009) Hum Reprod Update , vol.15 , pp. 139-151
    • Wright, C.F.1    Burton, H.2
  • 25
    • 33749539870 scopus 로고    scopus 로고
    • Use of bi-allelic insertion/deletion polymorphisms as a positive control for fetal genotyping in maternal blood: First clinical experience
    • DOI 10.1196/annals.1368.016, Circulating Nucleic Acids in Plasma and Serum IV
    • Page-Christiaens GC, Bossers B, van der Schoot CE, DE Haas M: Use of bi-allelic insertion/ deletion polymorphisms as a positive control for fetal genotyping in maternal blood: first clinical experience. Ann NY Acad Sci. 2006;1075:123-129. (Pubitemid 44532774)
    • (2006) Annals of the New York Academy of Sciences , vol.1075 , pp. 123-129
    • Page-Christiaens, G.C.M.L.1    Bossers, B.2    Van Der, S.C.E.3    De Haas, M.4
  • 28


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.