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Volumn 8, Issue 11, 2000, Pages 861-868
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Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9
a a b b c d d d e f g h a a b c a a |
Author keywords
FANCG XRCC9; Fanconi anaemia; Founder mutation; Mutation screening
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Indexed keywords
LEUCINE ZIPPER PROTEIN;
ALLELE;
ARTICLE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
FAMILY STUDY;
FANCONI ANEMIA;
GENE DELETION;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC POLYMORPHISM;
GENETIC SCREENING;
GENETIC VARIABILITY;
GERMANY;
HEMATOLOGIC DISEASE;
HOMOZYGOSITY;
HUMAN;
MISSENSE MUTATION;
MOLECULAR CLONING;
NUCLEOTIDE SEQUENCE;
PATHOGENESIS;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN STRUCTURE;
SEQUENCE ANALYSIS;
SEQUENCE HOMOLOGY;
STOP CODON;
AMINO ACID SEQUENCE;
BASE SEQUENCE;
DNA;
DNA MUTATIONAL ANALYSIS;
DNA-BINDING PROTEINS;
FANCONI ANEMIA;
FANCONI ANEMIA COMPLEMENTATION GROUP G PROTEIN;
HUMANS;
MOLECULAR SEQUENCE DATA;
MUTATION;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
SEQUENCE HOMOLOGY, AMINO ACID;
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EID: 0033710326
PISSN: 10184813
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.ejhg.5200552 Document Type: Article |
Times cited : (55)
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References (25)
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