Prenatal detection of rhesus D genotype [2]

Lancet

Volumn 349, Issue 9051, 1997, Pages 540-

  Hamlington, Jeanette ^a   Cunningham, Joan ^a   Mason, Gerald ^a   Mueller, Robert ^a   Miller, David ^a,b  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MESSENGER RNA; RHESUS D ANTIBODY; RNA;

CLINICAL ARTICLE; CLINICAL TRIAL; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DNA DETERMINATION; EMBRYO CELL; ERYTHROCYTE; ERYTHROID CELL; HIGH RISK PREGNANCY; HUMAN; LETTER; LEUKOCYTE; MATERNAL BLOOD; NEWBORN HEMOLYTIC DISEASE; PHENOTYPE; PLACENTA; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RNA ANALYSIS; SEROCONVERSION; TROPHOBLAST;

EID: 0342547009     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(97)80090-6     Document Type: Article

References (5)

1. Tovey LAD. Haemolytic disease of the newborn and its prevention. In: Contrerus C, ed. ABC of transfusion. London: BMJ Publishing Group, 1992: 22-25.
2. Bowman JM. The prevention of Rh immunization. Transfus Med Rev 1988; 2: 129-50.
3. Lo YMD, Bowell PJ, Selinger M, et al. Prenatal determination of fetal RhD status by analysis of peripheral blood of rhesus negative mothers. Lancet 1993; 341: 1147-48.
4. Simsek S, Faas BH, Bleeker PM, et al. Rapid RhD genotyping by polymerase chain reaction-based amplification of DNA. Blood 1995; 85: 2975-80.
5. Lo YMD, Noakes PJ, Fleming KA, Wainscoat JS. Detection of fetal RhD sequence from peripheral blood of sensitised RhD-negative pregnant women. Br J Haematol 1994: 87: 658-60.