Prenatal diagnosis of the fetal RhD blood type using a single fetal nucleated erythrocyte from maternal blood

Obstetrics and Gynecology

Volumn 87, Issue 4, 1996, Pages 501-505

  Sekizawa, Akihiko ^a   Watanabe, Akira ^b   Kimura, Takehiko ^b   Saito, Hiroshi ^b   Yanaihara, Takumi ^b   Sato, Takeshi ^b  

^a National Center for Global Health and Medicine   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BLOOD GROUP RH; BLOOD GROUP TYPING; BLOOD SAMPLING; CLINICAL ARTICLE; ERYTHROCYTE; FEMALE; HUMAN; MATERNAL BLOOD; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0029947544     PISSN: 00297844     EISSN: None     Source Type: Journal    
DOI: 10.1016/0029-7844(95)00496-3     Document Type: Article

References (16)

1. Douglas GW, Thomas L, Carr M, Cullen M, Morris R. Trophoblast in the circulating blood during pregnancy. Am J Obstet Gynecol 1959;78:960-73.
2. Naeslund J. Undersökningar over placentas permeabilitet med tillhjälp av bl.a. blodgruppsbestämnigar, radioaktivt märkta blodkroppar och elliptocyter. Nordik Medicin 1946;29:589-92.
3. Herzenberg LA, Bianchi DW, Schröder J, Cann HM, Iverson GM. Fetal cells in the blood of pregnant women: Detection and enrichment by fluorescence-activated cell sorting. Proc Natl Acad Sci U S A 1979;76:1453-5.
4. Bianchi DW, Flint AF, Pizzimenti MF, Knoll JHM, Latt SA. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc Natl Acad Sci USA 1990;87:3279-83.
5. Bianchi DW, Shuber AP, DeMaria MA, Fougner AC, Klinger KW. Fetal cells in maternal blood: Determination of purity and yield by quantitative polymerase chain reaction. Am J Obstet Gynecol 1994;171:922-6.
6. Takabayashi H, Kuwabara S, Ukita T, Ikawa K, Yamafuji K, Igarashi T. Development of non-invasive fetal DNA diagnosis from maternal blood. Prenat Diagn 1995;15:74-7.
7. Zhang L, Cui X, Schmitt K, Hubert R, Navidi W, Arnheim N. Whole genome amplification from a single cell: Implications for genetic analysis. Proc Natl Acad Sci U S A 1992;89:5847-51.
8. Li H, Cui X, Arnheim N. Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction. Proc Natl Acad Sci U S A 1990;87: 4580-4.
9. Chong SS, Kristjansson K, Cota J, Handyside AH, Hughes MR. Preimplantation prevention of X-linked disease: Reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified ZFX and ZFY sequences. Hum Mol Genet 1993;2:1187-91.
10. Kristjansson K, Chong SS, Van den Veyver IB, Subramanian S, Snabes MC, Hughes MH. Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification. Nature Genet 1994;6:19-23.
11. Van den Veyver IB, Chong SS, Cota J, Bennett PR, Fisk NM, Handyside AH, et al. Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn. Am J Obstet Gynecol 1995;172: 533-40.
12. Bowman JM, Pollock JM. Failures of intravenous Rh immune globulin prophylaxis: An analysis of the reasons for such failures. Transfus Med Rev 1987;1:101-2.
13. Mac Gregor SN, Silver RK, Sholl JS. Enhanced sensitization after cordocentesis in a rhesus-isoimmunized pregnancy. Am J Obstet Gynecol 1991;165:382-3.
14. Spinnato JA. Hemolytic disease of the fetus: A plea for restraint. Obstet Gynecol 1992;80:873-7.
15. Bennett PR, Le Van Kim C, Colin Y, Warwick RM, Cherif-Zahar B, Fisk NM, et al. Prenatal determination of fetal RhD type by DNA amplification. N Engl J Med 1993;329:607-10.
16. Yamakawa Y, Oka H, Hori S, Arai T, Izumi R. Detection of human parvovirus B19 DNA by nested polymerase chain reaction. Obstet Gynecol 1995;86:126-9.