Determination of miR-373 and miR-204 levels in neuronal exosomes in Alzheimer’s disease von TAŞDELEN, Elifcan, ÖZEL KIZIL, Erguvan Tuğba, TEZCAN, Sabiha, YALAP, Eray, BİNGÖL, Ayşe Petek, YÜRÜR KUTLAY, Nüket

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Importance of patient selection criteria in determining diagnostic copy number variations in patients with multiple congenital anomaly/mental retardation von Altıner, Şule, Kutlay, Nüket Yürür

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Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment von Kaymak Cihan, Meriç, Karabulut, Halil Gürhan, Yürür Kutlay, Nüket, Ilgın Ruhi, Hatice, Tükün, Ajlan, Olcay, Lale

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A Paternal "Balanced" Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings von Gökoğlu, Mustafa, Yürür Kutlay, Nüket, Altıner, Şule

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Diagnostic challenges in a family with dominant dystrophic epidermolysis bullosa and isolated hereditary nail disorder: paternal gonosomal mosaicism for COL7A1 variant and maternal... von Öktem, Ayşe, Özaydın, Berna, Gündüz, Kaan, Gökpınar İli, Ezgi, Şanlı, Hatice, Kaplan, İbrahim, Yürür Kutlay, Nüket

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Mosaic Small Supernumerary Marker Chromosome Derived from Five Discontinuous Regions of Chromosome 8 in a Patient with Neutropenia and Oral Aphthous Ulcer von Altiner, Sule, Kutlay, Nuket Yurur, Ruhi, Hatice Ilgin

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The association between telomere length and ischemic stroke risk and phenotype von Yetim, Ezgi, Topcuoglu, Mehmet Akif, Yurur Kutlay, Nuket, Tukun, Ajlan, Oguz, Kader K., Arsava, Ethem Murat

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Which has greater effects on leukomogenesis in Philadelphia chromosome positive leukemias: fusion or cell type? von Yurur-kutlay, Nuket, Tukun, Ajlan

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Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4 von Turhan, Nihan, Yürür-Kutlay, Nüket, Topcuoglu, Pervin, Saykı, Müyesser, Yüksel, Meltem, Gürman, Günhan, Tükün, Ajlan

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New Homozygous Missense MSMO1 Mutation in Two Siblings with SC4MOL Deficiency Presenting with Psoriasiform Dermatitis von Kalay Yildizhan, Incilay, Gökpınar İli, Ezgi, Onoufriadis, Alexandros, Kocyigit, Pelin, Kesidou, Evangelia, Simpson, Michael A., McGrath, John A., Kutlay, Nüket Yürür, Kundakci, Nihal

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Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche von Erdeve, Senay Savas, Berberoglu, Merih, Yurur-Kutlay, Nüket, Sıklar, Zeynep, Hacıhamdıoglu, Bulent, Tukun, Ajlan, Ocal, Gonul

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Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family von Taşdelen, Elifcan, Calame, Daniel G., Akay, Gulsen, Mitani, Tadahiro, Fatih, Jawid M., Herman, Isabella, Du, Haowei, Coban‐Akdemir, Zeynep, Marafi, Dana, Jhangiani, Shalini N., Posey, Jennifer E., Gibbs, Richard A., Altıparmak, Taylan, Kutlay, Nüket Yürür, Lupski, James R., Pehlivan, Davut

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Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia von Kiraz, Aslıhan, Sezer, Ozlem, Alemdar, Adem, Canbek, Sezin, Duman, Nilgun, Bisgin, Atıl, Cora, Tulin, Ruhi, Hatice Ilgın, Ergoren, Mahmut Cerkez, Geçkinli, Bilgen Bilge, Sag, Sebnem Ozemri, Gözden, Hilmi Erdem, Oz, Ozlem, Altıntaş, Zuhal Mert, Yalcıntepe, Sinem, Keskin, Adem, Tak, Ayşegül Yabacı, Paskal, Şeyma Aktaş, Yürekli, Uğur Fahri, Demirtas, Mercan, Evren, Emine Unal, Hanta, Abdullah, Başdemirci, Müşerref, Suer, Kaya, Balta, Burhan, Kocak, Nadir, Karabulut, Halil Gürhan, Cobanogulları, Havva, Ateş, Esra Arslan, Bozdoğan, Sevcan Tuğ, Eker, Damla, Ekinci, Sadiye, Nergiz, Süleyman, Tuncalı, Timur, Yagbasan, Serap, Alavanda, Ceren, Kutlay, Nuket Yurur, Evren, Hakan, Erdoğan, Murat, Altıner, Sule, Sanlidag, Tamer, Gonen, Gizem Akıncı, Vicdan, Arzu, Eras, Nazan, Eker, Hatice Koçak, Balasar, Ozgür, Tuncel, Gulten, Dundar, Munis, Gurkan, Hakan, Temel, Sehime Gulsun

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A child with myelodysplastic syndrome with hypocellular fibrosis von Akyay, Arzu, Olcay, Lale, Kuzu, Işınsu, Bozdoğan, Nazan, Ünal-İnce, Elif, İleri, Talia, Tükün, Ajlan, Yürür-Kutlay, Nuket

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Association Between N363S and Bcl/Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment von Cihan, Meriç Kaymak, Karabulut, Halil Gürhan, Kutlay, Nüket Yürür, Ruhi, Hatice Ilgın, Tükün, Ajlan, Olcay, Lale

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An Evaluation of the Phenotypic Features of Fanconi Anemia Together with DEB/MMC Positivity in 199 Turkish Patients von YÜRÜR-KUTLAY, Nüket, TUNCALİ, Timur, ILGIN-RUHİ, Hatice, KARABULUT, Halil Gürhan, TUKUN, Ajlan

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An Evaluation of the Phenotypic Features of Fanconi Anemia Together with DEB/MMC Positivity in 199 Turkish Patients/Fanconi Anemisinin Fenotipik Özelliklerinin DEB/MMC Pozitifligi... von Yürür-Kutlay, Nüket, Tuncali, Timur, Ilgin-Ruhi, Hatice, Karabulut, Halil Gürhan, Tukun, Ajlan

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Prognostic impact of RUNX1 and ETV6 gene copy number on pediatric B-cell precursor acute lymphoblastic leukemia with or without hyperdiploidy von Kutlay, Nuket Yurur, Pekpak, Esra, Altıner, Sule, Ileri, Talia, Vicdan, Arzu Nedime, Dinçaslan, Handan, Ince, Elif Unal, Tukun, Fatma Ajlan

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Akut Miyeloid Lösemide Kromozomal Anomaliler: Tek Merkezden 417 Olgunun Sitogenetik Sonuçları von Nüket, TUNCALI, YÜRÜR-KUTLAY

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A Paternal "Balanced" Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings von Gökoğlu, Mustafa, Yürür Kutlay, Nüket, Altıner, Şule

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