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Cancer Genet Cytogenet ; 102(2): 148-50, 1998 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-9546070

RESUMEN

Cytogenetics and fluorescence in situ hybridization (FISH) of a hepatoblastoma are presented. The results of standard chromosome analysis were as follows: 47,XY,+2,add(4)(q35),-9,+20[10]. FISH with the use of whole-chromosome paints revealed partial trisomy of the long arm of chromosome 2 by insertion into chromosome 9. Comparison of the G-banded metaphases with metaphase FISH led to a reinterpretation of the karyotype as: 47,XY,add(4)(q35),der(9)ins(9;2)(p22;q?21q?25),+20. This case supports previous observations that the critical region of trisomy 2 lies between 2q21 and 2qter and shows how partial trisomy 2q may evade detection in G-banded metaphases.


Asunto(s)
Cromosomas Humanos Par 2 , Cromosomas Humanos Par 9 , Hepatoblastoma/genética , Neoplasias Hepáticas/genética , Trisomía , Preescolar , Bandeo Cromosómico , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Masculino
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