Resultados de procura - Tuğba Kontbay

Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants por Tuğba Kontbay, İhsan Turan

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Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment por Tuğba Kontbay, Zeynep Şıklar, Serdar Ceylaner, Merih Berberoğlu

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Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases por Zeynep Şıklar, Tuğba Kontbay, Kevin Colclough, Kashyap A. Patel, Merih Berberoğlu

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