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GJB2-RELATED NON-SYNDROMIC HEARING LOSS VARIANTS’ SPECTRUM AND THEIR FREQUENCY IN TURKISH POPULATION.
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- Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2022, v. 85, n. 2, p. 162, doi. 10.26650/IUITFD.1011501
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- Article
Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
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- Turkish Journal of Neurology / Turk Noroloji Dergisi, 2021, v. 17, n. 3, p. 240, doi. 10.4274/tnd.2021.91298
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- Article
TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features.
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- European Journal of Neurology, 2021, v. 28, n. 8, p. 2603, doi. 10.1111/ene.14908
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- Article
NOONAN SENDROMU’NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ.
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- Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2021, v. 84, n. 1, p. 34, doi. 10.26650/IUITFD.2020.803356
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- Article
Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family.
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- Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2018, v. 55, n. 1, p. 98, doi. 10.5152/npa.2017.19484
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- Article