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

Volltext

Assessment of whole-exome sequencing results in neurogenetic diseases von Balasar, Özgür, Başdemirci, Müşerref

Volltext

A rare variant Klinefelter syndrome seen 40 years later: 47,X,del(Xq24),Y von Özkent, Mehmet Serkan, Balasar, Özgür

Volltext

Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report von Ciftciler, Rafiye, Balasar, Özgur, Keyik, Hilal, Ciftciler, Ali Erdinc

Volltext

Investigation of the interchromosomal effects in male carriers with structural chromosomal abnormalities using FISH von Balasar, Özgür, Acar, Hasan

Volltext

Status dystonicus associated with CLN8 disease von Yıldırım, Miraç, Köse, Engin, Keçeli, Avni Merter, Balasar, Özgür, Şimşek, Nazmi

Volltext

Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey von Balasar, Özgür, Kadıoğlu Yılmaz, Banu, Başdemirci, Müşerref, Koçak Eker, Hatice, Eser Çavdartepe, Büşra, Şimşek, Levent, Tunçez, Ebru, Duymuş, Fahrettin

Volltext

Mild congenital myopathy due to a novel variation in SPEG gene von Yildirim, Mirac, Balasar, Ozgur, Kose, Engin, Dogan, Melih Timucin

Volltext

The effect of rs9939609 FTO gene polymorphism on weight loss after laparoscopic sleeve gastrectomy von Balasar, Özgür, Çakır, Tuğrul, Erkal, Özgür, Aslaner, Arif, Çekiç, Bülent, Uyar, Mehmet, Bülbüller, Nurullah, Oruç, Mehmet Tahir

Volltext

Male infertility associated with de novo pericentric inversion of chromosome 1 von Balasar, Özgür, Zamani, Ayşe Gül, Balasar, Mehmet, Acar, Hasan

Volltext

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.

Volltext

A rare CALR variant mutation and efficient peginterferon alfa-2a response in a patient with essential thrombocythemia von Ciftciler, Rafiye, Balasar, Ozgur

Volltext

Distinct Distribution of HBB Variants in Two Cohorts of Beta Thalassemia Patients, and a Novel Variant from Turkey von Kocak Eker, Hatice, Balasar, Ozgur

Volltext

HLA-B51 in Patients with Recurrent Aphthous Stomatitis von OZDEMIR, Mustafa, ACAR, Hasan, DENIZ, Fatma, TÜMER, Emrah, ENGIN, Burhan, BALASAR, Ozgür

Volltext

Tüm Ekzom Dizileme Verilerinde İkincil Bulguların Retrospektif Olarak Değerlendirilmesi von Balasar, Özgür, Başdemirci, Müşerref

Volltext

Herediter Meme Kanseri Tanılı ve Riskli Bireylerde BRCA1/BRCA2 Sonuçlarının Değerlendirilmesi: Varyant Frekansı, Dağılımı ve Dört Yeni Varyant (Retrospektif Kohort Çalışması)... von Başdemirci, Müşerref, Balasar, Özgür

Volltext

Lenz-Majewski syndrome and recurrent otitis media: Are they related or not? von Maden Bedel, Fayize, Balasar, Özgür, Erol Aytekin, Selma, Keleş, Sevgi, Çaksen, Hüseyin

Volltext

A Case of Mosaic 45,X/46,XY Infertile Man with an AZF Deletion von Balasar, Mine, Tasdemir, Pelin, Balasar, Özgür, Göktas, Emine

Volltext

A rare CALR variant mutation and efficient peginterferon alfa-2a response in a patient with essential thrombocythemia von Ciftciler, Rafiye, Balasar, Ozgur

Volltext

Mild congenital myopathy due to a novel variation in SPEG gene von Yildirim, Mirac, Balasar, Ozgur, Kose, Engin, Dogan, Melih Timucin

Volltext