Fluorescence in situ hybridization detection of two telomeres on the short arm of a derived chromosome 16 in an infant with thrombocytopenia

Cancer Genetics and Cytogenetics

Volumn 120, Issue 2, 2000, Pages 99-104

  Gribble, S ^a   Andrews, K ^b   Williams, D ^b   Tillett, A ^b   Bloxham, D ^b   Proffit, J ^d   Hackbarth, M ^d   Grace, C ^c   Green, A ^a   Nacheva, E ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b ADDENBROOKE S HOSPITAL   (United Kingdom)

^c Digital Scientific Ltd   (United Kingdom)

^d ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BONE MARROW; CASE REPORT; CHROMOSOME 16; CHROMOSOME ABERRATION; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; CYTOGENETICS; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; NEWBORN; PRIORITY JOURNAL; TELOMERE; THROMBOCYTOPENIA;

BONE MARROW CELLS; CHROMOSOME BANDING; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 3; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; TELOMERE; THROMBOCYTOPENIA; TRANSLOCATION, GENETIC;

EID: 0034661273     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00259-9     Document Type: Article

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