Browsing by Author "Genç, Nimetullah Mete"

Now showing items 1-4 of 4

Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism

Cangül, Hakan; Özel, Mavi Deniz; Genç, Nimetullah Mete; Kardelen Al, Aslı Derya; Darendeliler, Feyza (Nature Publishing Group, 2018)

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Exome sequencing in a large family with Tourette Syndrome/Chronic Tic Disorder

Özel, Mavi Deniz; Gönenli Toker, Sinem; Ağargün, Mehmet Yücel; Fışkırma, I. A.; Çaralan, Erdal Fırat; Genç, Nimetullah Mete; Cangül, Hakan; Üstek, Duran (Nature Publishing Group, 2018)

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A novel candidate frameshift mutation for catecholaminergic polymorphic ventricular tchycardia

Işık, Fatma Büşra; Sözügüzel, Mavi Deniz; Genç, Nimetullah Mete; Çaralan, E. F.; Doğru, Zübeyir; Akdeniz, Coşkun; Tuzcu, Volkan; Cangül, Hakan (Nature Publishing Group, 2019)

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A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome

Sözügüzel, Mavi Deniz; Işık, Fatma Büşra; Genç, Nimetullah Mete; Çaralan, E. F.; Doğru, Zübeyir; Akdeniz, Coşkun; Cangül, Hakan (Nature Publishing Group, 2019)

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