TRISOMY 12, 17p (P53) DELETION AND 14q32 (IgH) IN B-CELL CHRONIC LYMPHOCYTIC LEUKEMIA: CLINICAL AND IMMUNOPHENOTYPIC CORRELATION

Safaa Mohamed Abd EI-Gaber;

Abstract


T
he B-cell chronic lymphocytic leukemia (CLL) is a disease with a very low proliferative activity. It is characterized by the accumulation of clonal B-lymphocytes that seem to be arrested in early G0/G1 phase of the cell-cycle. Although the pathogenesis


Other data

Title TRISOMY 12, 17p (P53) DELETION AND 14q32 (IgH) IN B-CELL CHRONIC LYMPHOCYTIC LEUKEMIA: CLINICAL AND IMMUNOPHENOTYPIC CORRELATION
Other Titles دراسة تثلث الكروموزم 12 وتلاشى للجين 53 بالذراع القصير للكروموزوم ٧ 1 و العيوب فى الذراع الطويل للكروموزوم 1٤ في مرض ابيضاض الدم الليمفاوى المزمن "ب" وعلاقتهم بالتصنيف الخلوى المناعى و الحالة الإكلينيكية للمرض
Authors Safaa Mohamed Abd EI-Gaber
Keywords TRISOMY 12, 17p (P53) DELETION AND 14q32 (IgH) IN B-CELL CHRONIC LYMPHOCYTIC LEUKEMIA: CLINICAL AND IMMUNOPHENOTYPIC CORRELATION
Issue Date 2010
Description 
T
he B-cell chronic lymphocytic leukemia (CLL) is a disease with a very low proliferative activity. It is characterized by the accumulation of clonal B-lymphocytes that seem to be arrested in early G0/G1 phase of the cell-cycle. Although the pathogenesis

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