Prenatal genotyping of Jka and Jkb of the human Kidd blood group system by allele-specific polymerase chain reaction

Prenatal Diagnosis

Volumn 18, Issue 12, 1998, Pages 1225-1231

  Hessner, Martin J ^a   Pircon, Richard A ^b   Johnson, Susan T ^a   Luhm, Robert A ^a  

^a BLOOD RESEARCH INSTITUTE   (United States)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

Haemolytic disease of the newborn (HDN); Kidd blood group; Polymerase chain reaction (PCR); Prenatal testing

Indexed keywords

PRIMER DNA;

ALLELE; AMNIOCENTESIS; AMNION CELL; ARTICLE; BLOOD; BLOOD GROUP KIDD SYSTEM; CONTROLLED STUDY; FEMALE; FETUS CELL; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MATERNAL BLOOD; NEWBORN HEMOLYTIC DISEASE; NUCLEOTIDE SEQUENCE; OLIGONUCLEOTIDE PROBE; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL SCREENING; PRIORITY JOURNAL; RISK FACTOR; SEROTYPE;

ADULT; ALLELES; AMNIOCENTESIS; DNA; DNA PRIMERS; ERYTHROBLASTOSIS, FETAL; FEMALE; GENOTYPE; HUMANS; INFANT, NEWBORN; KIDD BLOOD-GROUP SYSTEM; POLYMERASE CHAIN REACTION; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; PRENATAL DIAGNOSIS; REPRODUCIBILITY OF RESULTS; SEROTYPING;

EID: 0032436376     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199812)18:12<1225::AID-PD434>3.0.CO;2-D     Document Type: Article

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