Fluorescence in situ hybridization: uses and limitations (Q34079185)

30 July 2017

title

Fluorescence in situ hybridization: uses and limitations (English)

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30 July 2017

2

Le Beau MM

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30 July 2017

Gozzetti A

1

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30 July 2017

publication date

1 October 2000

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30 July 2017

language of work or name

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Seminars in Hematology

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30 July 2017

volume

37

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30 July 2017

issue

4

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30 July 2017

page(s)

320-333

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publication type of scholarly work

30 July 2017

review article

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A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

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7 January 2021

High incidence of cryptic translocations involving the Ig heavy chain gene in multiple myeloma, as shown by fluorescence in situ hybridization

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Fish analysis at diagnosis in acute lymphoblastic leukemia

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Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

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The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALL

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Genetic abnormalities in chronic lymphocytic leukemia and their clinical and prognostic implications

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Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis

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7 January 2021

Cytogenetic abnormalities in multiple myeloma

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Interphase cytogenetics in chronic lymphocytic leukemia

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7 January 2021

Prognostic relevance of monosomy at the 13q14 locus detected by fluorescence in situ hybridization in B-cell chronic lymphocytic leukemia

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High incidence of deletions but infrequent inactivation of the retinoblastoma gene in human myeloma cells

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Cloning and gene mapping of the chromosome 13q14 region deleted in chronic lymphocytic leukemia

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7 January 2021

The impact of the new fish technologies on the cytogenetics of haematological malignancies

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2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences

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Heterogeneity in telomere length of human chromosomes.

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Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization

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Oncogenic Transcription Factors in the Human Acute Leukemias

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7 January 2021

Multiple fluorescence in situ hybridization.

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7 January 2021

Padlock probes reveal single-nucleotide differences, parent of origin and in situ distribution of centromeric sequences in human chromosomes 13 and 21

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Two 22q telomere deletions serendipitously detected by FISH

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Fluorescence in situ hybridization: molecular probes for diagnosis of pediatric neoplastic diseases

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7 January 2021

The prognostic significance of 13q14 deletions in chronic lymphocytic leukemia

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Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization

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7 January 2021

10.1016/S0037-1963(00)90013-1

Identifiers

DOI

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30 July 2017

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