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Monosomy 13

A chromosomal abnormality consisting of the absence of a copy (homolog) of chromosome 13.
National Institutes of Health

Papers overview

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2007
2007
Purpose: Two pathways, hyperdiploid and nonhyperdiploid, are proposed for progression to plasma cell neoplasia. Implication of… Expand
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Highly Cited
2005
Highly Cited
2005
The clinical efficacy of evaluating genetic anomalies in metaphase cells versus interphase nuclei for multiple myeloma (MM) is… Expand
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Highly Cited
2001
Highly Cited
2001
Primary plasma cell leukemia (PCL) is a rare plasma cell malignancy. Consequently, few large reports have been published… Expand
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Highly Cited
2000
Highly Cited
2000
Interphase fluorescence in situ hybridization (FISH) studies of chromosomal region 13q14 were performed to investigate the… Expand
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2000
2000
Chromosome 13 abnormalities are frequently observed in multiple myeloma (MM). Several reports recently demonstrated the strong… Expand
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Highly Cited
2000
Highly Cited
2000
Since deletion of chromosome 13q is a clinically relevant feature in multiple myeloma (MM), we analyzed bone marrow plasma cells… Expand
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Highly Cited
1999
Highly Cited
1999
Chromosomal abnormalities are present in most (if not all) patients with multiple myeloma (MM) and primary plasma cell leukemia… Expand
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Highly Cited
1999
Highly Cited
1999
Clonal plasma cells in monoclonal gammopathy of undetermined significance (MGUS) have been shown to bear copy number chromosome… Expand
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Highly Cited
1998
Highly Cited
1998
Recent observations indicate that chromosome aberrations are important prognostic factors in patients with multiple myeloma (MM… Expand
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Highly Cited
1988
Highly Cited
1988
Karyotypic abnormalities were studied in multiple myeloma and were correlated with clinical features. Among 115 evaluable… Expand
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