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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

http://www.wikidata.org/entity/Q37924989

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Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM090 Current Role of Genetics in Hematologic Malignancies.

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

http://www.wikidata.org/entity/Q37924989

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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type

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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prefLabel

The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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J.1751-553X.2011.01364.X

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International Journal of Laboratory Hematology

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The role of molecular genetic analysis within the diagnostic haemato-oncology laboratory.

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High resolution melting for mutation scanning of TP53 exons 5-8

BRAF mutations in hairy-cell leukemia

Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays

Recurring mutations found by sequencing an acute myeloid leukemia genome

Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

PCR-based methods for the enrichment of minority alleles and mutations

Relation of gene expression phenotype to immunoglobulin mutation genotype in B cell chronic lymphocytic leukemia

One-step detection of c-kit point mutations using peptide nucleic acid-mediated polymerase chain reaction clamping and hybridization probes

Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML.

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10.1111/J.1751-553X.2011.01364.X

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2011-08-26T00:00:00Z

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