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Among CLL patiens with multiple fish abnormatities, 13Q and 11Q deletions entail the commonest combination in contrast to 11Q and 17P deletions, being the combination with worse outcome

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dc.contributor.authorGonzález-Gascón Y Marín, I
dc.contributor.authorHernández, JA
dc.contributor.authorHernánez-Sanchez, M
dc.contributor.authorRodriguez-Vicente, AE
dc.contributor.authorPuiggros, A
dc.contributor.authorCollado, R
dc.contributor.authorLuño, E
dc.contributor.authorGonzález, T
dc.contributor.authorRuiz-Xivillé, N
dc.contributor.authorOrtega, M
dc.contributor.authorGimeno, E
dc.contributor.authorMuñoz, C
dc.contributor.authorInfante, MS
dc.contributor.authorDelgado, J
dc.contributor.authorAventín, A
dc.contributor.authorVargas, MT
dc.contributor.authorGonzález, M
dc.contributor.authorBosch, F
dc.contributor.authorEspinet, B
dc.contributor.authorHernández-Rivas, JM
dc.contributor.authoraffiliation[González-Gascón Y Marín,I; Hernández,JA] Medicine, Universidad Complutense de Madrid,Spain. [González-Gascón Y Marín,I; Hernández,JA; Muñoz,C; Infante,MS] Hematology, Hospital Universitario Infanta Leonor, MADRID,Spain. [Hernánez-Sanchez,M; Rodriguez-Vicente,AE; Hernández-Rivas,LM] Centro de Investigación del Cáncer-IBMCC, Universidad de Salamanca, (USAL-CSIC), Salamanca, Spain. [Puiggros,A; Gimeno,E; Espinet,B] Laboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain. [Puiggros,A] Grup de Recerca Translacional en Neoplàsies Hematològiques, Programa de Recerca en Càncer, Institut Hospital del Mar d’Investigacions Mèdiques (IMIM), Barcelona, Spain. [Collado,R] Hematology, Consorcio Hospital General Universitario, Valencia, Spain. [Luño,E] Hematology, Hospital Universitario Central de Asturias, Oviedo, Spain. [González,T] Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain. [Ruiz-Xivillé,N] Laboratori Hematologia, ICO-Hospital Germans Trias i Pujol, Institut de Recerca Contra la Leucèmia Josep Carreras (IJC), Universitat Autònoma de Barcelona, Barcelona, Spain. [Ortega,M] Laboratorio de Citogenética y Servicio de Hematología, Hospital Vall d’Hebron, Barcelona, Spain. [Delgado,J] 11Hematology, Hospital Clinic and Institut d’Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. [Aventín,A] Hematología, Hospital Sant Pau, Barcelona, Spain. [Vargas,MT] Hospital Universitario Virgen de la Macarena,Sevilla, Spain. [González,M; Hernández-Rivas,JM] Hematologia, IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain. [Bosch,F] Hematology, Hospital Vall d’Hebron, Barcelona, Spain.es
dc.date.accessioned2016-10-27T11:25:20Z
dc.date.available2016-10-27T11:25:20Z
dc.date.issued2016-06-09
dc.description.abstractFluorescence in-situ hybridization (FISH) defines a hierarchy of genetic changes that predicts survival in CLL. However, multiple abnormalities (MA) may also occur and little is known about its distribution and clinical impact. containing clinical and biological data.es
dc.description.versionYeses
dc.identifier.citationGonzález-Gascón Y Marín I, Hernández JA, Hernánez-Sanchez M, Rodriguez-Vicente AR, Puiggros A, Collado R, et al. Among CLL patiens with multiple fish abnormatities, 13Q and 11Q deletions entail the commonest combination in contrast to 11Q and 17P deletions, being the combination with worse outcome. Haematologica. 2016; 101(s1), pag.429es
dc.identifier.essn1592-8721
dc.identifier.issn0390-6078
dc.identifier.urihttp://hdl.handle.net/10668/2496
dc.journal.titleHaematologica
dc.language.isoen
dc.publisherFerrata Storti Foundationes
dc.relation.publisherversionhttp://haematologica.org/content/101/s1es
dc.rights.accessRightsopen access
dc.subjectAnomalías múltipleses
dc.subjectAberraciones cromosómicases
dc.subjectFluorescenciaes
dc.subjectHibridación fluorescente in situes
dc.subject.meshMedical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Congenital Abnormalities::Abnormalities, Multiplees
dc.subject.meshMedical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Variation::Mutation::Chromosome Aberrationses
dc.subject.meshMedical Subject Headings::Phenomena and Processes::Physical Phenomena::Magnetic Phenomena::Electromagnetic Phenomena::Electromagnetic Radiation::Light::Luminescence::Fluorescencees
dc.subject.meshMedical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humanses
dc.subject.meshMedical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Cytological Techniques::Histocytological Preparation Techniques::Staining and Labeling::In Situ Hybridization::In Situ Hybridization, Fluorescencees
dc.titleAmong CLL patiens with multiple fish abnormatities, 13Q and 11Q deletions entail the commonest combination in contrast to 11Q and 17P deletions, being the combination with worse outcomees
dc.typeconference presentation
dc.type.hasVersionVoR
dspace.entity.typePublication

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