RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotype

Prenatal Diagnosis

Volumn 19, Issue 5, 1999, Pages 424-427

  Denomme, Gregory A ^a,b   Akoury, Hani ^c   Sermer, Mathew ^c   Kelton, John G ^d  

^a MOUNT SINAI HOSPITAL   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY HEALTH NETWORK   (Canada)

^d MCMASTER UNIVERSITY MEDICAL CENTRE   (Canada)

Author keywords

Genotype phenotype discrepancy; Haemolytic disease of the newborn; RhD PCR

Indexed keywords

RHESUS D ANTIBODY;

ADULT; AMNION FLUID; ARTICLE; BLOOD GROUP RHESUS SYSTEM; CASE REPORT; CHORION VILLUS; DEVICE; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DNA DETERMINATION; ETHNIC GROUP; FEMALE; FETUS RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HEMOLYTIC ANEMIA; HUMAN; HUMAN TISSUE; LABORATORY TEST; MALE; MATERNAL BLOOD; MOLECULAR CLONING; NEWBORN; NUCLEOTIDE SEQUENCE; PARENT; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 0032907055     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199905)19:5<424::AID-PD562>3.0.CO;2-7     Document Type: Article

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