Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene von Hallıoğlu Kılınç, Olgu, Giray, Dilek, Bişgin, Atıl, Tuğ Bozdoğan, Sevcan, Karpuz, Derya

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BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history von Bisgin, Atil, Boga, Ibrahim, Yalav, Orcun, Sonmezler, Ozge, Tug Bozdogan, Sevcan

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Hereditary Spastic Paraplegia Type 26 with a Novel Mutation in B4GALNT1 Gene and Literature Review of the Clinical Features von Incecık, Faruk, Herguner, Ozlem M, Bozdogan, Sevcan Tug

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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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Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey von Bozdogan, Sevcan Tug, Mujde, Cem, Boga, Ibrahim, Sonmezler, Ozge, Hanta, Abdullah, Rencuzogullari, Cagla, Ozcan, Dilek, Altintas, Derya Ufuk, Bisgin, Atil

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Hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features von Incecik, Faruk, Besen, Seyda, Bozdogan, Sevcan

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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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Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey von Bisgin, Atil, Sag, Sebnem Ozemri, Dogan, Muhammet E., Yildirim, Mahmut S., Gumus, Aydeniz Aydin, Akkus, Nejmiye, Balasar, Ozgur, Durmaz, Ceren D., Eroz, Recep, Altiner, Sule, Alemdar, Adem, Aliyeva, Lamia, Boga, Ibrahim, Cam, Fethi S., Dogan, Berkcan, Esbah, Onur, Hanta, Abdullah, Mujde, Cem, Ornek, Cemre, Ozer, Sinem, Rencuzogullari, Cagla, Sonmezler, Ozge, Bozdogan, Sevcan Tug, Dundar, Munis, Temel, Sehime G.

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Identification of a novel mutation in GRIN2A gene with global developmental delay and refractory epilepsy von Sarigecili, Esra, Direk, Meltem, Komur, Mustafa, Bozdogan, Sevcan, Okuyaz, Cetin

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No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children von Bozdogan, Sevcan Tug, Kutuk, Meryem Ozlem, Tufan, Evren, Altıntaş, Zuhal, Temel, Gülhan Orekici, Toros, Fevziye

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A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey von Boga, Ibrahim, Ozemri Sag, Sebnem, Duman, Nilgun, Ozdemir, Sevda Yesim, Ergoren, Mahmut Cerkez, Dalci, Kubilay, Mujde, Cem, Parsak, Cem Kaan, Rencuzogullari, Cagla, Sonmezler, Ozge, Yalav, Orcun, Alemdar, Adem, Aliyeva, Lamiya, Bozkurt, Ozlem, Cetintas, Sibel, Cubukcu, Erdem, Deligonul, Adem, Dogan, Berkcan, Ornek Erguzeloglu, Cemre, Evrensel, Turkkan, Gokgoz, Sehsuvar, Senol, Kazim, Tolunay, Sahsine, Akyurek, Esra, Basgoz, Neslihan, Gökçe, Nuriye, Dundar, Bilge, Ozturk, Figen, Taskin, Duygu, Demirtas, Mercan, Cag, Murat, Diker, Omer, Olgun, Polat, Tug Bozdogan, Sevcan, Dundar, Munis, Bisgin, Atil, Temel, Sehime Gulsun

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Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants von Gök, Veysel, Leblebisatan, Göksel, Gürlek Gökçebay, Dilek, Güler, Salih, Doğan, Muhammet Ensar, Tuğ Bozdoğan, Sevcan, Koca Yozgat, Ayça, Özcan, Alper, Pekpak Şahinoğlu, Esra, Tokgöz, Hüseyin, Çil, Metin, Özemri Sağ, Şebnem, Yilmaz, Ebru, Şaşmaz, Hatice İlgen, Evim, Melike Sezgin, Akbayram, Sinan, Karadoğan, Meriban, Mutlu, Fatma Türkan, Boğa, İbrahim, Yeter Doğan, Burcu, Yarali, Neşe, Çalişkan, Ümran, Bişgin, Atil, Temel, Şehime Gülsün, Proven, Melanie, Gibson, Kate, Demir, Büşra Şeniz, Saraçoğlu, Hatice, Eken, Ahmet, Karakükçü, Çiğdem, Karakükçü, Musa, Güneş, Adalet Meral, Özbek, Namık Yaşar, Kilinç, Yurdanur, Patiroğlu, Türkan, Özdemir, Mehmet Akif, Roy, Noemi B A, Ünal, Ekrem

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Early diagnostic clues of mucolipidosis type II: Significance of radiological findings von Burgac, Ezgi, Kaplan, İrem, Köseci, Burcu, Kara, Esra, Kor, Deniz, Bulut, Fatma Derya, Atmış, Anıl, Pişkin, Ferhatcan, Tuğ Bozdoğan, Sevcan, Urel Demir, Gizem, İncecik, Faruk, Önenli Mungan, Neslihan

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Abstract 5294: Clinical utility of a multigene panel for hematologic malignancies von Bozdogan, Sevcan Tug, Rencuzogullari, Cagla, Mujde, Cem, Bisgin, Atil

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Abstract 3125: Disturbance of CALR mutation profile in MPNs by NGS and Real-Time PCR von Rencuzogullari, Cagla, Bozdogan, Sevcan Tug, Guvenc, Birol, Bisgin, Atil

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Meta-analysis and single-center experience on the comprehensive genomic characterization and landscape of BRCA1 and BRCA2 in Turkey von Bisgin, Atil, Boga, Ibrahim, Sonmezler, Ozge, Mujde, Cem, Hanta, Abdullah, Tug Bozdogan, Sevcan

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Thrombus prevalence and risk factors in critically ill pediatric patients

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Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes von Yuan, Bo, Pehlivan, Davut, Karaca, Ender, Patel, Nisha, Charng, Wu-Lin, Gambin, Tomasz, Gonzaga-Jauregui, Claudia, Sutton, V Reid, Yesil, Gozde, Bozdogan, Sevcan Tug, Tos, Tulay, Koparir, Asuman, Koparir, Erkan, Beck, Christine R, Gu, Shen, Aslan, Huseyin, Yuregir, Ozge Ozalp, Al Rubeaan, Khalid, Alnaqeb, Dhekra, Alshammari, Muneera J, Bayram, Yavuz, Atik, Mehmed M, Aydin, Hatip, Geckinli, B Bilge, Seven, Mehmet, Ulucan, Hakan, Fenercioglu, Elif, Ozen, Mustafa, Jhangiani, Shalini, Muzny, Donna M, Boerwinkle, Eric, Tuysuz, Beyhan, Alkuraya, Fowzan S, Gibbs, Richard A, Lupski, James R

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A Case with Mental Retardation, Gynecomastia and Dysmorphic Features von Ozge Ozalp Yuregir, Huseyin Aslan, Sevcan Tug Bozdogan, Muhammed Hamza Muslumanoglu

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COL12A1 Gene Variant and a Review of the Literature: A Case Report of Ullrich Congenital Muscular Dystrophy von İpek, Rojan, Çavdartepe, Büşra Eser, Bozdoğan, Sevcan Tuğ, Yiş, Uluç

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