Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin von Bayram, Yavuz, Karaca, Ender, Coban Akdemir, Zeynep, Yilmaz, Elif Ozdamar, Tayfun, Gulsen Akay, Aydin, Hatip, Torun, Deniz, Bozdogan, Sevcan Tug, Gezdirici, Alper, Isikay, Sedat, Atik, Mehmed M, Gambin, Tomasz, Harel, Tamar, El-Hattab, Ayman W, Charng, Wu-Lin, Pehlivan, Davut, Jhangiani, Shalini N, Muzny, Donna M, Karaman, Ali, Celik, Tamer, Yuregir, Ozge Ozalp, Yildirim, Timur, Bayhan, Ilhan A, Boerwinkle, Eric, Gibbs, Richard A, Elcioglu, Nursel, Tuysuz, Beyhan, Lupski, James R

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Gene expression changes in bioceramic paste-treated human dental pulp cells von Torun, Deniz, Torun, Zeynep Ö., Demirkaya, Kadriye, Sarper, Meral, Elçi, Mualla P., Avcu, Ferit

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Effects of triethylene glycol dimethacrylate (TEGDMA) on the odontoclastic differentiation ability of human dental pulp cells von Öncel Torun, Zeynep, Torun, Deniz, Baykal, Barış, Öztuna, Ali, Yeşildal, Fatih, Avcu, Ferit

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey von Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

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Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report... von Torun, Deniz, Arslan, Mutluay, Yüksel, Zafer

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High frequency of MEFV gene mutations in patients with myeloid neoplasm von Oktenli, Cagatay, Sayan, Ozkan, Celik, Serkan, Erikci, Alev A., Tunca, Yusuf, Terekeci, Hakan M., Umur, Elcin Erkuvan, Sanisoglu, Yavuz S., Torun, Deniz, Tangi, Fatih, Sahan, Burak, Nalbant, Selim

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Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey von Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

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The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery von Yilmaz, Sedat, Erdem, Hakan, Tunay, Servet, Torun, Deniz, Genc, Halil, Tunca, Yusuf, Karadag, Omer, Simsek, Ismail, Bahce, Muhterem, Pay, Salih, Dinc, Ayhan

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Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome von Torun, Deniz, Arslan, Mutluay, Çavdarlı, Büşranur, Akar, Hatice, Cram, David Stephen

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Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia von Torun, Deniz, Nevruz, Oral, Akyol, Mesut, Kozan, Salih, Bahçe, Muhterem, Güran, Sefik, Beyan, Cengiz

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Mitochondrial complex I and III mRNA levels in bipolar disorder von Akarsu, Süleyman, Torun, Deniz, Erdem, Murat, Kozan, Salih, Akar, Hatice, Uzun, Ozcan

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Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy von Olgac, Asburce, Kasapkara, Cigdem Seher, Kilic, Mustafa, Keskin, Ebru Yılmaz, Sandal, Gonca, Cram, David Stephen, Häberle, Johannes, Torun, Deniz

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Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time von Öncel Torun, Zeynep, Torun, Deniz, Demirkaya, Kadriye, Yavuz, Süleyman Tolga, Sarper, Meral, Avcu, Ferit

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POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum von Rossi, Alessandra, Blok, Lot Snijders, Neuser, Sonja, Klöckner, Chiara, Platzer, Konrad, Faivre, Laurence Olivier, Weigand, Heike, Dentici, Maria L, Tartaglia, Marco, Niceta, Marcello, Alfieri, Paolo, Srivastava, Siddharth, Coulter, David, Smith, Lacey, Vinorum, Kristin, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Torun, Deniz, Arslan, Mutluay, Lauridsen, Mathilde F, Murch, Oliver, Irving, Rachel, Lynch, Sally A, Mehta, Sarju G, Carmichael, Jenny, Zonneveld-Huijssoon, Evelien, de Vries, Bert, Kleefstra, Tjitske, Johannesen, Katrine M, Westphall, Ian T, Hughes, Susan S, Smithson, Sarah, Evans, Julie, Dudding-Byth, Tracy, Simon, Marleen, van Binsbergen, Ellen, Herkert, Johanna C, Beunders, Gea, Oppermann, Henry, Bakal, Mert, Møller, Rikke S, Rubboli, Guido, Bayat, Allan

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POU3F3‐related disorder: Defining the phenotype and expanding the molecular spectrum von Rossi, Alessandra, Blok, Lot Snijders, Neuser, Sonja, Klöckner, Chiara, Platzer, Konrad, Faivre, Laurence Olivier, Weigand, Heike, Dentici, Maria L., Tartaglia, Marco, Niceta, Marcello, Alfieri, Paolo, Srivastava, Siddharth, Coulter, David, Smith, Lacey, Vinorum, Kristin, Cappuccio, Gerarda, Brunetti‐Pierri, Nicola, Torun, Deniz, Arslan, Mutluay, Lauridsen, Mathilde F., Murch, Oliver, Irving, Rachel, Lynch, Sally A., Mehta, Sarju G., Carmichael, Jenny, Zonneveld‐Huijssoon, Evelien, Vries, Bert, Kleefstra, Tjitske, Johannesen, Katrine M., Westphall, Ian T., Hughes, Susan S., Smithson, Sarah, Evans, Julie, Dudding‐Byth, Tracy, Simon, Marleen, Binsbergen, Ellen, Herkert, Johanna C., Beunders, Gea, Oppermann, Henry, Bakal, Mert, Møller, Rikke S., Rubboli, Guido, Bayat, Allan

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Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype von Rosti, Rasim O., Karaer, Kadri, Karaman, Birsen, Torun, Deniz, Guran, Sefik, Bahce, Muhterem

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Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical features von Akarsu, Süleyman, Torun, Deniz, Bolu, Abdullah, Erdem, Murat, Kozan, Salih, Ak, Mehmet, Akar, Hatice, Uzun, Özcan

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Karyotype Analysis Results in Girls Followed with Short Stature von TORUN, Deniz, AKIN, Onur, KAVUŞ, Haluk, ÖZTUNA, Ali, AKAR, Hatice, TUNCA, Yusuf

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Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts von Torun, Deniz, Bahce, Muhterem, Alanbay, Ibrahim, Guran, Sefik, Baser, Iskender

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FMF hastalarındaki MEFV gen mutasyon sıklığı ve mutasyonların dağılımı: Tek bir merkezden geniş bir hasta grubunun analizi von Torun, Deniz, Tekgöz, Emre, Kavuş, Haluk, Öztuna, Ali, Akar, Hatice, Çınar, Muhammet, Yılmaz, Sedat, Güran, Şefik, Tunca, Yusuf

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