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Trisomy 4

A chromosomal abnormality consisting of the presence of a third copy of chromosome 4 in somatic cells.
National Institutes of Health

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2013
2013
Waldenström's macroglobulinemia is a disease of mature B cells, the genetic basis of which is poorly understood. Few recurrent… Expand
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2012
2012
Acute myeloid leukemia (AML) with isolated trisomy 4 is rare. Associations with KIT mutations on chromosome 4q12 have been… Expand
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Review
2005
Review
2005
The Kasumi-1 cell line is an intensively investigated model system of Acute Myeloid Leukemia with t(8;21) translocation, that… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND AND OBJECTIVES Mutations of KIT receptor tyrosine kinase are involved in the constitutive activation and development… Expand
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2003
2003
t(8;21)(q22;q22) is the most frequently observed karyotypic abnormality associated with acute myeloid leukemia (AML), especially… Expand
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2003
2003
inhibitor of angiogenesis. Proc Natl Acad Sci 1994; 91: 4082–4085. 7 Corral LG, Haslett PA, Muller GW, Chen R, Wong LM, Ocampo CJ… Expand
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2001
2001
Two cases of trisomy 4 mosaicism are reported including one with molecularly confirmed uniparental disomy (UPD) of chromosome 4… Expand
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2000
2000
A G-->T transversion at nucleotide 2467 of the c-KIT gene leading to Asp816-->Tyr (D816Y) substitution in the phosphotransferase… Expand
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2000
2000
The specific association of trisomy 4 and double minutes (dmin) is rare and is usually reported in patients with acute myeloid… Expand
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1993
1993
The expression of c-kit and its ligand, the stem cell factor (SCF), was studied in five cases of acute myeloid leukemia. One of… Expand
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