del(7)(p11-15) solely

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dc.contributor.author Zamecnikova, Adriana -
dc.date.accessioned 2018-11-08T09:41:10Z
dc.date.available 2018-11-08T09:41:10Z
dc.date.issued 2018 -
dc.identifier.citation Adriana, Zamecnikova. del(7)(p11-15) solely. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018, 7, p. 298-302 -
dc.identifier.issn 1768-3262 -
dc.identifier.uri http://hdl.handle.net/2042/68922
dc.description.abstract Complete or partial loss of chromosome 7 is a recurrent cytogenetic abnormality that may be observed in both de novo and therapy-related hematopoietic disorders. It predominantly presents as monosomy 7 or deletion of the long arm of chromosome 7, often associated with an unfavorable prognosis. Deletions of the short arm of chromosome 7, originated from either a terminal or an interstitial deletion are less frequent and their pathological significance is less well characterized. en
dc.language.iso en -
dc.publisher ARMGHM - Atlas Génétique des Cancers -
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Anomalies/del7pID1796.html -
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology en
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation -
dc.subject Monosomy 7 en
dc.subject 7p deletions en
dc.subject gene deletions en
dc.subject tumor suppressor genes en
dc.subject.classification Leukaemia Section en
dc.title del(7)(p11-15) solely en
dc.type Article -
dc.contributor.affiliation Kuwait Cancer Control Center, Department of Hematology, Laboratory of Cancer Genetics, Kuwait -
dc.identifier.doi https://doi.org/10.4267/2042/68922


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