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Mutational analysis of the neurofibromatosis type 1 gene in childhood myelodysplastic syndromes using a protein truncation assay.

Methods in molecular medicine - 1 Jan 2002

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Share to Bone Marrow Cells
Share to DNA Mutational Analysis
Share to DNA Primers
Share to Electrophoresis, Polyacrylamide Gel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Neurofibromatosis 1

Share to Leukocytes, Mononuclear

Share to Myelodysplastic Syndromes

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PMID: 11901500
DOI: 10.1385/1-59259-135-3:157

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Mutational analysis of the neurofibromatosis type 1 gene in childhood myelodysplastic syndromes using a protein truncation assay.PMID 11901500Read ↗

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Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.Semantic proximity Read ↗

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Identification of an insertion and accompanying deletion in exon 31 of the neurofibromatosis type 1 gene.Semantic proximity Read ↗

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Mutation scanning for the clinical laboratory-protein truncation test.Semantic proximity Read ↗

The protein truncation test in mutation detection and molecular diagnosis.Semantic proximity Read ↗

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