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- 2018
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Mark
Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2
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- Contribution to journal › Article
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The hidden genomic and transcriptomic plasticity of giant marker chromosomes in cancer
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- Contribution to journal › Article
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Mark
A Single Bout of Electroacupuncture Remodels Epigenetic and Transcriptional Changes in Adipose Tissue in Polycystic Ovary Syndrome
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- Contribution to journal › Article
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
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- Contribution to journal › Article
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Mark
Genetic predisposition to infection in a case of atypical hemolytic uremic syndrome
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- Contribution to journal › Article
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Mark
Internal tandem duplication mutations in the tyrosine kinase domain of FLT3 display a higher oncogenic potential than the activation loop D835Y mutation
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- Contribution to journal › Article
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Mark
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
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- Contribution to journal › Article
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Mark
Heritability of End-Stage Renal Disease : A Swedish Adoption Study
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- Contribution to journal › Article
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Bortezomib-induced peripheral neuropathy : A genome-wide association study on multiple myeloma patients
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- Contribution to journal › Article
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De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia
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- Contribution to journal › Article