Severe vitamin B(12) deficiency with pancytopenia, hepatosplenomegaly and leukoerythroblastosis in two Syrian refugee infants: a challenge to differentiate from acute leukaemia

Por Belen, Burcu, Hismi, Burcu Ozturk, Kocak, Ulker
Publicado em 2014

A Rare Galactosemia Complication: Vitreous Hemorrhage

Por Takci, Sahin, Kadayifcilar, Sibel, Coskun, Turgay, Yigit, Sule, Hismi, Burcu
Publicado em 2011

Pregnancy and Lactation Outcomes in a Turkish Patient with Lysinuric Protein Intolerance

Por Ünal, Özlem, Coşkun, Turgay, Orhan, Diclehan, Tokatl, Ayşegül, Dursun, Ali, Hişmi, Burcu, Özyüncü, Özgür, Sivri, Serap Hatice Kalkanoğlu
Publicado em 2013

Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Por Tekin, Mustafa , Hişmi, Burcu Öztürk , Fitoz, Suat , Özdağ, Hilal , Cengiz, Filiz Başak , Sırmacı, Aslı , Aslan, İdil , İnceoğlu, Bora , Yüksel-Konuk, E. Berrin , Yılmaz, Seda Taşır , Yasun, Öztan , Akar, Nejat 
Publicado em 2007

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

Por Sırmacı, Aslı, Erbek, Seyra, Price, Justin, Huang, Mingqian, Duman, Duygu, Cengiz, F. Başak, Bademci, Güney, Tokgöz-Yılmaz, Suna, Hişmi, Burcu, Özdağ, Hilal, Öztürk, Banu, Kulaksızoğlu, Sevsen, Yıldırım, Erkan, Kokotas, Haris, Grigoriadou, Maria, Petersen, Michael B., Shahin, Hashem, Kanaan, Moien, King, Mary-Claire, Chen, Zheng-Yi, Blanton, Susan H., Liu, Xue Z., Zuchner, Stephan, Akar, Nejat, Tekin, Mustafa
Publicado em 2010