RT Conference Proceedings
T1 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
A1 González-Gascón Y Marín, I
A1 Hernández, JA
A1 Hernánez-Sanchez, M
A1 Rodriguez-Vicente, AE
A1 Puiggros, A
A1 Collado, R
A1 Luño, E
A1 González, T
A1 Ruiz-Xivillé, N
A1 Ortega, M
A1 Gimeno, E
A1 Muñoz, C
A1 Infante, MS
A1 Delgado, J
A1 Aventín, A
A1 Vargas, MT
A1 González, M
A1 Bosch, F
A1 Espinet, B
A1 Hernández-Rivas, JM
K1 Anomalías múltiples
K1 Aberraciones cromosómicas
K1 Fluorescencia
K1 Hibridación fluorescente in situ
AB Fluorescence 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.
PB Ferrata Storti Foundation
SN 0390-6078
YR 2016
FD 2016-06-09
LK http://hdl.handle.net/10668/2496
UL http://hdl.handle.net/10668/2496
LA en
NO González-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.429
DS RISalud
RD Apr 11, 2025