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t/gene-cbl

CBL gene

Discuss publications and research concerning the CBL gene.

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Related literature

CBL Syndrome With Granular Cell Tumor and café au lait macules: Expansion of the Phenotype.
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Calreticulin Type 26 Mutation in Myelofibrosis: A Rare Variant With Diagnostic Challenges.
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CBL-Mutated Juvenile Myelomonocytic Leukaemia With Loss of Heterozygosity on 11q Detected by Microarray: Not Always Such a Favourable Outcome.
CBL
The Role and Impact of Non-driver Gene Mutations in Myelofibrosis.
CBL
Clinical characteristics, genomic profiling, treatments, and outcomes of Langerhans cell sarcoma.
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[BCR::ABL-Negative Triple Negative Myeloproliferative Neoplasm --Review].
CBL
A microglia clonal inflammatory disorder in Alzheimer's disease.
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Yield of genetic evaluation in non-syndromic pediatric moyamoya patients.
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Genetic Study of HGF-MET Signaling Pathway in Primary Lymphedema Patients: Supporting Evidence for Loss of Function Variants in HGF.
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Generation of a human Juvenile myelomonocytic leukemia iPSC line, CHOPi001-A, with a mutation in CBL.
CBL

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