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Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.
Not available
S-EPMC6972977
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biostudies-literature
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Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.
Not available
S-EPMC5321238
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biostudies-literature
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Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia.
Not available
S-EPMC7843618
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biostudies-literature
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Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology.
Not available
S-EPMC6315026
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biostudies-literature
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Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci.
Not available
S-EPMC5253627
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biostudies-literature
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Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Not available
S-EPMC8556284
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biostudies-literature
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Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.
Not available
S-EPMC5303820
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biostudies-literature
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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Not available
S-EPMC5223092
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biostudies-literature
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Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration.
Not available
S-EPMC5294887
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biostudies-literature
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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
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S-EPMC6037202
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biostudies-literature
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