Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 214, Issue 2, 1989, Pages 215-222

  Kyoizumi, S ^a   Nakamura, N ^a   Takebe, H ^b   Tatsumi, K ^b   German, J ^c   Akiyama, M ^a  

^a RADIATION EFFECTS RESEARCH FOUNDATION   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c NEW YORK BLOOD CENTER   (United States)

Author keywords

Bloom's syndrome; Erythrocyte; Glycophorin; Somatic mutation frequency

Indexed keywords

GLYCOPHORIN A;

BLOOM SYNDROME; CANCER RISK; CASE REPORT; ERYTHROCYTE; HEREDITY; HUMAN; HUMAN CELL; PRIORITY JOURNAL; SOMATIC MUTATION;

ALLELES; ANTIBODIES, MONOCLONAL; BLOOM SYNDROME; CASE REPORT; ERYTHROCYTES; FEMALE; FLUORESCENT ANTIBODY TECHNIQUE; GENE FREQUENCY; GENOTYPE; GLYCOPHORIN; HUMAN; MALE; MUTATION; SIALOGLYCOPROTEINS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, NON-P.H.S.; VARIATION (GENETICS);

EID: 0024325920     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/0027-5107(89)90166-8     Document Type: Article

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