Der(6)t(1;6)(q21-23;p21.3): A specific cytogenetic abnormality in myelofibrosis with myeloid metaplasia

British Journal of Haematology

Volumn 130, Issue 2, 2005, Pages 229-232

  Dingli, David ^a   Grand, Francis H ^b,c   Mahaffey, Victor ^a   Spurbeck, Jack ^a   Ross, Fiona M ^b,c   Watmore, Ann E ^d   Reilly, John T ^d   Cross, Nicholas C P ^b,c   Dewald, Gordon W ^a   Tefferi, Ayalew ^a  

^a MAYO CLINIC   (United States)

^b SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^c UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^d ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

Author keywords

Chromosomes; Myelofibrosis; t(1; 6) translocation

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 1; CHROMOSOME 6; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; HUMAN; IN SITU HYBRIDIZATION; MAJOR CLINICAL STUDY; MYELOFIBROSIS; MYELOID METAPLASIA; PHENOTYPE; PRIORITY JOURNAL; SURVIVAL; CHROMOSOME BREAKAGE; CLINICAL TRIAL; FEMALE; GENE TRANSLOCATION; GENETICS; KARYOTYPING; MALE; MIDDLE AGED; MULTICENTER STUDY; PROSPECTIVE STUDY;

ADULT; AGED; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; HUMANS; KARYOTYPING; MALE; MIDDLE AGED; MYELOFIBROSIS; MYELOID METAPLASIA; PROSPECTIVE STUDIES; TRANSLOCATION, GENETIC;

EID: 24944565419     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2005.05593.x     Document Type: Article

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