Chromothripsis in uterine leiomyomas

New England Journal of Medicine

Volumn 369, Issue 22, 2013, Pages 2160-2161

  Markowski, Dominique N ^a   Bullerdiek, Jörn ^b  

^a UNIVERSITY OF BREMEN   (Germany)

^b UNIVERSITY OF ROSTOCK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HIGH MOBILITY GROUP A PROTEIN; HIGH MOBILITY GROUP A2 PROTEIN; RAD51 PROTEIN;

CHROMOSOME 7; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOTHRIPSIS; GENE MUTATION; GENE OVEREXPRESSION; GENETIC ASSOCIATION; GENETIC DISORDER; HMGA1 GENE; HMGA2 GENE; HUMAN; KARYOTYPE; LETTER; MED12 GENE; PRIORITY JOURNAL; TUMOR GENE; UTERUS MYOMA; CHROMOSOME 7Q; CHROMOSOME ABERRATION; CLONAL VARIATION; GENE SEQUENCE; PATHOGENESIS; PHENOMENOLOGY; RAD51B GENE; SEQUENCE ANALYSIS;

EID: 84888315562     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc1310230     Document Type: Letter

References (2)

1. Mehine M, Kaasinen E, Mäkinen N, et al. Characterization of uterine leiomyomas by whole-genome sequencing. N Engl J Med 2013;369:43-53.
2. Markowski DN, Bartnitzke S, Löning T, Drieschner N, Helmke BM, Bullerdiek J. MED12 mutations in uterine fibroids - their relationship to cytogenetic subgroups. Int J Cancer 2012;131:1528-36.