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Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.
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What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'Internal Medicine for Rare Genetic Syndromes'.
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Benefit of cochlear implantation in a patient with Myhre syndrome.
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Case Report: Improved Height in a Patient With Myhre Syndrome Using a Combination of Growth Hormone and Letrozole.
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SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome.
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Natural history and life-threatening complications in Myhre syndrome and review of the literature.
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