TRAPPC9-Related Intellectual Disability: Report of Two New Cases and Review of the Literature von Uctepe, Eyyup, Yesilyurt, Ahmet, Esen, Fatma Nisa, Tümer, Sait, Mancılar, Hanifenur, Sonmez, Fatma Mujgan

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Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly von Uctepe, Eyyup, Vona, Barbara, Esen, Fatma Nisa, Sonmez, F Mujgan, Smol, Thomas, Tümer, Sait, Mancılar, Hanifenur, Geylan Durgun, Dilan Ece, Boute, Odile, Moghbeli, Meysam, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Bakhshoodeh, Behnoosh, Kim, Hyung Goo, Maroofian, Reza, Yesilyurt, Ahmet

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KCNB1 frameshift variant caused inherited intellectual disability, developmental delay, and seizure von Uctepe, Eyyup, Esen, Fatma Nisa, Tümer, Sait, Mancılar, Hanifenur, Yeşilyurt, Ahmet

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Chromosome 1p status in neuroblastoma correlates with higher expression levels of miRNAs targeting neuronal differentiation pathway von Bagci, Ozkan, Tumer, Sait, Altungoz, Oguz

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Rapid identification of Helicobacter pylori and assessment of clarithromycin susceptibility from clinical specimens using FISH von Demiray‐Gürbüz, Ebru, Yılmaz, Özlem, Olivares, Asalia Z, Gönen, Can, Sarıoğlu, Sülen, Soytürk, Müjde, Tümer, Sait, Altungöz, Oğuz, Şimşek, İlkay, Perez Perez, Guillermo I

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Detection of Helicobacter pylori and Determination of Clarithromycin Susceptibility Using Formalin-Fixed, Paraffin-Embedded Gastric Biopsy Specimens by Fluorescence In Situ Hybridi... von Yilmaz, Özlem, Demiray, Ebru, Tümer, Sait, Altungöz, Oǧuz, Yörükoǧlu, Kutsal, Soytürk, Müjde, Şimşek, ?lkay

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KCNB1 frameshift variant caused inherited intellectual disability, developmental delay, and seizure von Uctepe, Eyyup, Esen, Fatma Nisa, Tümer, Sait, Mancılar, Hanifenur, Yeşilyurt, Ahmet

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Rapid identification of H elicobacter pylori and assessment of clarithromycin susceptibility from clinical specimens using FISH von Demiray‐Gürbüz, Ebru, Yılmaz, Özlem, Olivares, Asalia Z, Gönen, Can, Sarıoğlu, Sülen, Soytürk, Müjde, Tümer, Sait, Altungöz, Oğuz, Şimşek, İlkay, Perez Perez, Guillermo I

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Copy number status and mutation analyses of anaplastic lymphoma kinase ( ALK ) gene in 90 sporadic neuroblastoma tumors von Bagci, Ozkan, Tumer, Sait, Olgun, Nur, Altungoz, Oguz

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A Witteveen-Kolk Syndrome Patient with Reflux Disease and a de novo Deletion of the SIN3A Gene von Uctepe, Eyyup, Kandemir, Nefise, Bir, Firdevs Dinçsoy, Karhan, Asuman Nur, Tumer, Sait, Ondes, Emine Busra, Konuskan, Bahadır, Yesilyurt, Ahmet

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Analysis of sporadic neuroblastic tumors reveals a novel PHOX2B mutation in neuroblastoma von Caglar, Hasan Onur, Tumer, Sait, Olgun, Hatice Nur, Altungoz, Oguz

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Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly von Uctepe, Eyyup, Vona, Barbara, Esen, Fatma Nisa, Sonmez, F Mujgan, Smol, Thomas, Tümer, Sait, Mancılar, Hanifenur, Geylan Durgun, Dilan Ece, Boute, Odile, Moghbeli, Meysam, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Bakhshoodeh, Behnoosh, Kim, Hyung Goo, Maroofian, Reza, Yesilyurt, Ahmet

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The Detection of Genetic Parameters for Prognostic Stratification of Neuroblastoma Using Multiplex Ligation-Dependent Probe Amplification Technique von Tumer, Sait, Altungoz, Oguz, Bagci, Ozkan, Olgun, H Nur

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Correlation of modified Shimada classification with MYCN and 1p36 status detected by fluorescence in situ hybridization in neuroblastoma von Altungoz, Oguz, Aygun, Nevim, Tumer, Sait, Ozer, Erdener, Olgun, Nur, Sakizli, Meral

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