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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
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
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
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
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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Review
1995
Review
1995
Secondary chromosomal aberrations were surveyed in non-Hodgkin's lymphomas (NHL) reported in the literature with one of the… 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
Highly Cited
1988
Highly Cited
1988
Cytogenetic analysis was performed in 47 newly diagnosed patients with agnogenic myeloid metaplasia (AMM); 32 had a normal… Expand
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