Bloom's syndrome - XVIII. Hypermutability at a tandem-repeat locus

Human Genetics

Volumn 90, Issue 4, 1992, Pages 360-367

  Groden, Joanna ^a   German, James ^a  

^a Weill Cornell Graduate School of Biomedical Sciences   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

ARTICLE; BLOOM SYNDROME; CHROMOSOME BANDING PATTERN; CONTROLLED STUDY; DNA POLYMORPHISM; GENE LOCUS; GENE MUTATION; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; LYMPHOCYTE CLONE; PRIORITY JOURNAL; SISTER CHROMATID EXCHANGE;

BASE SEQUENCE; BLOOM SYNDROME; CELL LINE, TRANSFORMED; CHILD; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 1; DNA; DNA PROBES; HUMAN; KARYOTYPING; MALE; MOLECULAR SEQUENCE DATA; MUTATION; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0027051362     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00220459     Document Type: Article

References (21)

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12. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA
13. Frequency of variant erythrocytes at the glycophorin A locus in two Bloom's syndrome patients
14. Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome
15. DNA fingerprinting of 7,12-dimethylbenz[a]anthracene-induced and spontaneous CD-1 mouse liver tumors
16. Characterization of a human ‘midisatellite’ sequence
17. Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p (D1S57)
18. Identification of colon cancer-predisposed individuals: A cytogenetic analysis
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21. Molecular characterization of a spontaneously generated new allele at a VNTR locus: No exchange of flanking DNA sequence