Silicone gel sheet dressing for sclerodermatous type chronic graftversus- host-disease (cGVHD) von Dinçer, Süleyman L, Kargı, Eksal, Dinçer, Sibel, Fitoz, Filiz, Akan, Hamdi

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Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development von Bademci, Guney, Abad, Clemer, Cengiz, Filiz B., Seyhan, Serhat, Incesulu, Armagan, Guo, Shengru, Fitoz, Suat, Atli, Emine Ikbal, Gosstola, Nicholas C., Demir, Selma, Colbert, Brett M., Seyhan, Gozde Cosar, Sineni, Claire J., Duman, Duygu, Gurkan, Hakan, Morton, Cynthia C., Dykxhoorn, Derek M., Walz, Katherina, Tekin, Mustafa

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FOXF2 is required for cochlear development in humans and mice von Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Elian, Fahed, Reyahi, Azadeh, Diaz-Horta, Oscar, Cengiz, Filiz B, Sineni, Claire J, Seyhan, Serhat, Atli, Emine Ikbal, Basmak, Hikmet, Demir, Selma, Nik, Ali Moussavi, Footz, Tim, Guo, Shengru, Duman, Duygu, Fitoz, Suat, Gurkan, Hakan, Blanton, Susan H, Walter, Michael A, Carlsson, Peter, Walz, Katherina, Tekin, Mustafa

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

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Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development von Bademci, Guney, Abad, Clemer, Cengiz, Filiz B, Seyhan, Serhat, Incesulu, Armagan, Guo, Shengru, Fitoz, Suat, Atli, Emine Ikbal, Gosstola, Nicholas C, Demir, Selma, Colbert, Brett M, Seyhan, Gozde Cosar, Sineni, Claire J, Duman, Duygu, Gurkan, Hakan, Morton, Cynthia C, Dykxhoorn, Derek M, Walz, Katherina, Tekin, Mustafa

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Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development von Bademci, Guney, Abad, Clemer, Cengiz, Filiz B, Seyhan, Serhat, Incesulu, Armagan, Guo, Shengru, Fitoz, Suat, Atli, Emine Ikbal, Gosstola, Nicholas C, Demir, Selma, Colbert, Brett M, Seyhan, Gozde Cosar, Sineni, Claire J, Duman, Duygu, Gurkan, Hakan, Morton, Cynthia C, Dykxhoorn, Derek M, Walz, Katherina, Tekin, Mustafa

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Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene von Tekin, Mustafa, Cengiz, Filiz Başak, Ayberkin, Eda, Kendirli, Tanıl, Fitoz, Suat, Tutar, Ercan, Çiftçi, Ergin, Conba, Atakan

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Evaluation and Outcome of Antenatal Hydronephrosis: A Prospective Study von Gökaslan, Filiz, Yalç nkaya, Fato, Fitöz, Suat, Özçakar, Z. Birsin

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Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations von Sırmacı, Aslı, Duman, Duygu, Öztürkmen-Akay, Hatice, Erbek, Seyra, İncesulu, Armağan, Öztürk-Hişmi, Burcu, Arıcı, Z. Serap, Yüksel-Konuk, E. Berrin, Taşır-Yılmaz, Seda, Tokgöz-Yılmaz, Suna, Cengiz, Filiz Başak, Aslan, İdil, Yıldırım, Müzeyyen, Hasanefendioğlu-Bayrak, Aylin, Ayçiçek, Abdullah, Yılmaz, İsmail, Fitoz, Suat, Altın, Fazilet, Özdağ, Hilal, Tekin, Mustafa

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Cardiovascular findings in a boy with arterial tortuosity syndrome: case report and review of the literature von Ekici, Filiz, Uçar, Tayfun, Fitöz, Suat, Atalay, Semra, Tutar, Ercan

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SLC26A4 mutations are associated with a specific inner ear malformation von Fitoz, Suat, Sennaroğlu, Levent, İncesulu, Armağan, Cengiz, Filiz Başak, Koç, Yasemin, Tekin, Mustafa

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Magnetic resonance angiographic and three-dimensional computerized tomographic identification of scimitar syndrome in an 8-month-old infant von Tutar, Ercan, Fitöz, Suat, Atalay, Semra, Uysalel, Adnan, Aral, Atilla, Ekici, Filiz, Eyileten, Zeynep B, Kendirli, Tanil

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Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene von Tekin, Mustafa, Cengiz, Filiz Başak, Ayberkin, Eda, Kendirli, Tanıl, Fitoz, Suat, Tutar, Ercan, Çiftçi, Ergin, Conba, Atakan

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