Genome-wide arrays in routine diagnostics of hematological malignancies.
about
New and emerging factors in tumorigenesis: an overviewHuman molecular cytogenetics: From cells to nucleotidesSNPs Array Karyotyping in Non-Hodgkin LymphomaSomatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesisUse of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemiaDiagnostic interpretation of array data using public databases and internet sources.Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes.Microarray-based genomic profiling and in situ hybridization on fibrotic bone marrow biopsies for the identification of numerical chromosomal abnormalities in myelodysplastic syndrome.Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial.Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling.Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.The current state of molecular cytogenetics in cancer diagnosis.Duplication of subtelomeric regions in an adult with acute monocytic leukemia with an acquired jumping translocation involving 3q13.31-qterStudy on the association between the Arg194Trp polymorphism in the XRCC1 gene and the risk of hematological malignancies.What Is the Clinical Utility of Repeat SNP Array Testing in the Follow-up of Myeloid Neoplasms?: A Retrospective Analysis of 44 Patients With Serial SNP Arrays.A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients.Identify latent chromosomal aberrations relevant to myelodysplastic syndromes.Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.Genomic profiling of myeloma: the best approach, a comparison of cytogenetics, FISH and array-CGH of 112 myeloma cases.The use of arrays to detect copy-number variations in clinical practice
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Genome-wide arrays in routine diagnostics of hematological malignancies.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Genome-wide arrays in routine diagnostics of hematological malignancies.
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type
label
Genome-wide arrays in routine diagnostics of hematological malignancies.
@en
prefLabel
Genome-wide arrays in routine diagnostics of hematological malignancies.
@en
P2093
P2860
P356
P1433
P1476
Genome-wide arrays in routine diagnostics of hematological malignancies.
@en
P2093
Annet Simons
Birgit Sikkema-Raddatz
Jacqueline Schoumans
Nicole Claudia Konrad
Nicole de Leeuw
Rosalind J Hastings
P2860
P304
P356
10.1002/HUMU.22057
P577
2012-04-09T00:00:00Z