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Öğe A Homozygous IFNGR1 Mutation Revealed Rare Immunodeficiency Syndrome For A Patient Having Common Symptoms(Springernature, 2024) Sunar, Ilknur; Akalin, Ayse Busra; Akalin, Ibrahim; Demircioglu, Fatih; Alchalabi, Mohammed; Derin, Zeynep; Tavil, Betul[Abstract Not Available]Öğe Whole exome sequencing for diagnostics in muscular dystrophy: a case report(Springernature, 2024) Derin, Zeynep; Akalin, Ayse Busra; Simsek, Elif Eroglu; Sunar, Ilknur; Akalin, Ibrahim[Abstract Not Available]
