ASSOCIATION OF NF-1 AND MOYAMOYA SYNDROME : CASE REPORT
Karaman, Serap, Şahin, Şifa, Yıldız, Edibe Pembegül, Tanyıldız, Hikmet Gülşah, Barburoğlu, Mehmet, Turgut, Tutku, Yılmaz, Yasin, Karakaş, Zeynep, Tuğcu, Deniz, Ünüvar, Ayşegül
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Published in Hematology, Transfusion and Cell Therapy (01.10.2022)
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Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan Syndrome
Turgut, G. Tutku, Kalelioglu, Ibrahim Halil, Karaman, Volkan, Sarac Sivrikoz, Tugba, Karaman, Birsen, Uyguner, Zehra Oya, Kalayci, Tugba
Published in Molecular syndromology (01.04.2023)
Published in Molecular syndromology (01.04.2023)
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Manufacture of custom-made spectacles using three-dimensional printing technology
Altinkurt, Emre, Ceylan, Nihan Aksu, Altunoglu, Umut, Turgut, Gozde Tutku
Published in Clinical and experimental optometry (01.11.2020)
Published in Clinical and experimental optometry (01.11.2020)
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Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin‐B receptor (LBR)‐related regressive spondylometaphyseal dysplasia
Turgut, Gozde Tutku, Güleç, Çağrı, Sarac Sivrikoz, Tugba, Kale, Hamdi, Karaman, Birsen, Nishimura, Gen, Altunoglu, Umut
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures
Turgut, Gozde Tutku, Altunoglu, Umut, Gulec, Cagri, Sarac Sivrikoz, Tugba, Kalaycı, Tuğba, Toksoy, Guven, Avcı, Şahin, Yıldırım, Behiye Tuğçe, Sayın, Gözde Yeşil, Kalelioglu, Ibrahim Halil, Karaman, Birsen, Has, Recep, Başaran, Seher, Yuksel, Atil, Kayserili, Hülya, Uyguner, Zehra Oya
Published in Clinical genetics (01.06.2024)
Published in Clinical genetics (01.06.2024)
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Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosis
Altunoglu, Umut, Palencia-Campos, Adrian, Güneş, Nilay, Turgut, Gozde Tutku, Nevado, Julian, Lapunzina, Pablo, Valencia, Maria, Iturrate, Asier, Otaify, Ghada, Elhossini, Rasha, Ashour, Adel, K. Amin, Asmaa, Elnahas, Rania F, Fernandez-Nuñez, Elisa, Flores, Carmen-Lisset, Arias, Pedro, Tenorio, Jair, Chamorro Fernández, Carlos Israel, Güven, Yeliz, Özsu, Elif, Eklioğlu, Beray Selver, Ibarra-Ramirez, Marisol, Diness, Birgitte Rode, Burnyte, Birute, Ajmi, Houda, Yüksel, Zafer, Yıldırım, Ruken, Ünal, Edip, Abdalla, Ebtesam, Aglan, Mona, Kayserili, Hulya, Tuysuz, Beyhan, Ruiz-Pérez, Victor
Published in Journal of medical genetics (01.07.2024)
Published in Journal of medical genetics (01.07.2024)
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Clinical and molecular genetic findings of Crisponi/cold‐induced sweating syndrome (CS/CISS) spectrum in patients from Turkey
Yilmaz Gulec, Elif, Turgut, Gozde Tutku, Gezdirici, Alper, Karaman, Volkan, Ozturk, Fatma Nihal, Avci, Sahin, Kalayci, Tugba, Senturk, Leyli, Ayaz, Akif, Kayserili, Hulya, Uyguner, Zehra Oya, Altunoğlu, Umut
Published in Clinical genetics (01.09.2022)
Published in Clinical genetics (01.09.2022)
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Functional loss of ubiquitin‐specific protease 14 may lead to a novel distal arthrogryposis phenotype
Turgut, Gozde Tutku, Altunoglu, Umut, Sivrikoz, Tugba Sarac, Toksoy, Guven, Kalaycı, Tuğba, Avcı, Şahin, Karaman, Birsen, Gulec, Cagri, Başaran, Seher, Sayın, Gözde Yeşil, Kayserili, Hulya, Uyguner, Zehra Oya
Published in Clinical genetics (01.04.2022)
Published in Clinical genetics (01.04.2022)
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Journal Article
Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan Syndrome
Turgut, G Tutku, Kalelioglu, Ibrahim Halil, Karaman, Volkan, Sarac Sivrikoz, Tugba, Karaman, Birsen, Uyguner, Zehra Oya, Kalayci, Tugba
Published in Molecular syndromology (01.04.2023)
Published in Molecular syndromology (01.04.2023)
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Antenatal diagnostic dilemma in a pseudodominant pedigree with lamin-B receptor (LBR)-related regressive spondylometaphyseal dysplasia
Turgut, Gozde Tutku, Güleç, Çağrı, Sarac Sivrikoz, Tugba, Kale, Hamdi, Karaman, Birsen, Nishimura, Gen, Altunoglu, Umut
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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