Frequent monoallelic loss of D13S319 in multiple myeloma patients shown by interphase fluorescence in situ hybridization
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References (22)
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
1986 • 2,968 citations
Current Protocols in Human Genetics
2001 • 1,023 citations
Multiple Myeloma: Increasing Evidence for a Multistep Transformation Process
1998 • 761 citations
The clinical significance of cytogenetic studies in 100 patients with multiple myeloma, plasma cell leukemia, or amyloidosis
1985 • 419 citations
Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalities
1995 • 418 citations
Cytogenetic findings in 200 patients with multiple myeloma
1995 • 378 citations
Altered Expression of the Retinoblastoma Gene Product in Human Sarcomas
1990 • 221 citations
Plasma cell karyotype in multiple myeloma
1988 • 174 citations
MULTIPLE MYELOMA: ALMOST ALL PATIENTS ARE CYTOGENETICALLY ABNORMAL
1996 • 161 citations
Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance
1995 • 143 citations
The Genetic Basis of Cancer
1995 • 140 citations
13q deletions in lymphoid malignancies
1995 • 137 citations
Evidence for a new tumour suppressor locus (DBM) in human B–cell neoplasia telomeric to the retinoblastoma gene
1993 • 135 citations
Cloning and Gene Mapping of the Chromosome 13q14 Region Deleted in Chronic Lymphocytic Leukemia
1997 • 130 citations
High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics
1993 • 127 citations
Cellular DNA content as a marker of human multiple myeloma
1980 • 113 citations
Minimal region of loss at 13q14 in B-cell chronic lymphocytic leukemia
1996 • 112 citations
Chronic lymphocytic leukemia cells with allelic deletions at 13q14 commonly have one intact RB1 gene: evidence for a role of an adjacent locus.
1993 • 102 citations
Deletion of the retinoblastoma gene in multiple myeloma.
1994 • 90 citations
Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma.
1995 • 85 citations
Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization.
1995 • 66 citations
Detection of numerical aberrations in hematologic neoplasias by fluorescence in situ hybridization.
1997 • 16 citations