Human RhD(el) is caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene [9]

Blood

Volumn 92, Issue 7, 1998, Pages 2602-2604

  Chang, J G ^a   Wang, J C ^a   Yang, T Y ^a   Tsan, K W ^a   Shih, M C ^a   Peng, C T ^a   Tsai, C H ^a  

^a MACKAY MEMORIAL HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD GROUP RHESUS SYSTEM; CARBOXY TERMINAL SEQUENCE; DNA POLYMORPHISM; EXON; GENE DELETION; GENE EXPRESSION; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; AMINO ACID SEQUENCE; BIOSYNTHESIS; BLOOD GROUP TYPING; BLOOD TRANSFUSION; CHROMOSOME 1; GENETICS; INTRON; LABORATORY DIAGNOSIS; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RHESUS ISOIMMUNIZATION; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY;

ALLOANTIBODY; RHO(D) ANTIBODY; RHO(D) ANTIGEN;

AMINO ACID SEQUENCE; BASE SEQUENCE; BLOOD GROUPING AND CROSSMATCHING; BLOOD TRANSFUSION; CHROMOSOMES, HUMAN, PAIR 1; FALSE NEGATIVE REACTIONS; HUMANS; INTRONS; ISOANTIBODIES; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; RH ISOIMMUNIZATION; RH-HR BLOOD-GROUP SYSTEM; SEQUENCE ALIGNMENT; SEQUENCE DELETION; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 0032173426     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.7.2602     Document Type: Letter

References (5)