Molecular spectra of HPRT deletion mutations in circulating T- lymphocytes in Fanconi anemia patients

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 431, Issue 2, 1999, Pages 341-350

  Laquerbe, Agnès ^a   Sala Trepat, Maria ^a   Vives, Claude ^a   Escarceller, Monica ^a   Papadopoulo, Dora ^a  

^a INSTITUT CURIE   (France)

Author keywords

Deletion mutagenesis; Fanconi anemia; HPRT locus; T lymphocytes

Indexed keywords

ARTICLE; CHROMOSOME BREAKAGE; FANCONI ANEMIA; GENE DELETION; GENETIC LINKAGE; HUMAN; HUMAN CELL; PATHOGENESIS; PRIORITY JOURNAL; T LYMPHOCYTE;

ADOLESCENT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BREAKAGE; DNA NUCLEOTIDYLTRANSFERASES; FANCONI ANEMIA; GENE REARRANGEMENT, GAMMA-CHAIN T-CELL ANTIGEN RECEPTOR; HUMANS; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; INFANT; MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; T-LYMPHOCYTES; VDJ RECOMBINASES;

EID: 0033385037     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0027-5107(99)00177-3     Document Type: Article

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