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- W1566892359 abstract "Background and Objectives: To determine the most chromosomal abnormalities seen in Childhood Acute Lymphoblastic Leukemia (CALL) in Mosul, and to evaluate the correlations between clinical haematological and chromosomal abnormalities in CALL. Pateints and Methods: Clinical notes, haematological parameters and cytogenetic analysis were studied for all patients. Cases were collected from oncology unit at Ibn Al-Atheer Teaching Hospital (ATH) in Mosul. Results: The frequency of normal karyotype was (42.9%) while the frequency of pseudodiploidy, hyperdiploidy and hypodiploidy were (8.5%), (28.6%) and (20%), respectively. Cases with hyperdiploidy had significantly low Total Leukocyte Count (TLC), higher platelet count with (P<0.001), (P<0.05), respectively. Massive Hepato-Splenomegaly (MHS) was seen mainly in hypodiploidy group (P<0.01)." @default.
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- W1566892359 date "2011-09-27" @default.
- W1566892359 modified "2023-09-26" @default.
- W1566892359 title "Chromosomal Changes in Childhood Acute Lymphoblastic Leukemia in Mosul" @default.
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