Neslihan Düzkale Teker
4PUBLICATIONS
9CO-AUTHORS
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Publications (4)
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|Jun 23, 2022
Genetic Etiology of Ichthyosis in Turkish Patients: Next-generation Sequencing Identified Seven Novel MutationsHanife Saat, Ibrahim Sahin, Neslihan Duzkale
|Aug 16, 2021
Significant neuropsychiatric symptoms: three mucopolysaccharidosis type IIIB cases, two of whom were siblings with a novel NAGLU gene mutation.Aydan Değerliyurt, Özlem Yayıcı Köken, Neslihan Düzkale Teker
|Jul 28, 2021
Investigation of genotype-phenotype relationship in Turkish patients with inherited retinal disease by next generation sequencing.Neslihan Duzkale, Umut Arslan
|Apr 19, 2021
The Relationship of Mutation Carriage of <i>BRCA1/2</i> and Family History in Triple-Negative Breast Cancer: Experience from a Diagnostic Center in Turkey.Neslihan Duzkale, Olcay Kandemir
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