Abdullah Sezer
Publication Activity (10 Years)
Years Active: 2022-2024
Publications (10 Years): 11
Publications (10 Years): 11
Publications
- Abdullah Sezer, Zeynep Özdemir, Erdem Özkan, Semra Çetinkaya
- Tarik Duzenli, Abdullah Sezer, Ferda Emriye PercinLetter to the Editor regarding "New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant" by Kılıç and Koşukçu, "An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant" by Yüksel Ülker et al. and "Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings" by Duzenli et al. American journal of medical genetics. Part A (2023)
- Tarik Duzenli, Abdullah Sezer, Ferda Emriye PercinLetter to the Editor regarding "New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant" by Kılıç and Koşukçu, "An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant" by Yüksel Ülker et al. and "Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings" by Duzenli et al. American journal of medical genetics. Part A 194 (4) (2023)
- Tarik Duzenli, Abdullah Sezer, Ferda Emriye PercinLetter to the Editor regarding "New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant" by Kılıç and Koşukçu, "An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant" by Yüksel Ülker et al. and "Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings" by Duzenli et al. American journal of medical genetics. Part A 194 (4) (2023)
- Çağatay Günay, Duygu Aykol, Özlem Özsoy, Ece Sönmezler, Yaren Sena Hanci, Bulent Kara, Deniz Akkoyunlu Sünnetçi, Naci Cine, Adnan Deniz, Tolgahan Özer, Cemile Büşra Ölçülü, Özlem Yilmaz, Seda Kanmaz, Sanem Yilmaz, Hasan Tekgül, Nihal Yildiz, Elif Acar Arslan, Ali Cansu, Nihal Olgaç Dündar, Fatma Kusgoz, Elif Didinmez, Pinar Gencpinar, Tuğçe Aksu Uzunhan, Biray Ertürk, Alper Gezdirici, Akif Ayaz, Akgün Ölmez, Müge Ayanoğlu, Ayşe Fahriye Tosun, Yasemin Topçu, Betül Kılıç, Kursad Aydin, Ezgi Çağlar, Özlem Ersoy Kosvali, Cetin Okuyaz, Şeyda Besen, Leman Tekin Orgun, İlknur Erol, Deniz Yüksel, Abdullah Sezer, Ergin Atasoy, Ülkühan Öztoprak, Serdal Güngör, Bilge Ozgor, Meral Karadağ, Cengiz Dilber, Bahtiyar Şahinoğlu, Emek Uyur Yalçın, Nilüfer Eldes Hacifazlioglu, Ahmet Yaramiş, Pinar Edem, Hande Gazeteci Tekin, Ünsal Yilmaz, Aycan Ünalp, Sevim Turay, Didem Biçer, Gülen Gül Mert, İpek Dokurel Çetin, Serkan Kırık, Gülten Öztürk, Yasemin Karal, Aslıhan Sanri, Ayşe Aksoy, Muzaffer Polat, Nezir Özgün, Didem Soydemir, Gamze Sarikaya Uzan, Döndü Ülker Üstebay, Ayşen Gök, Mehmet Can Yeşilmen, Uluç Yaş, Gökhan Karakülah, Ahmet Bursali, Yavuz Oktay, A Semra Hiz
- Tarik Duzenli, Abdullah Sezer, Ferda Emriye PercinLetter to the Editor regarding "New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant" by Kılıç and Koşukçu, "An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant" by Yüksel Ülker et al. and "Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings" by Duzenli et al. American journal of medical genetics. Part A 194 (4) (2023)
- Tarik Duzenli, Abdullah Sezer, Gulsum Kayhan, Ayse Tana Arslan, Ferda E Percin
- Abdullah Sezer, Ferda Emriye Perçin, Hasan Huseyin Kazan, Gulsum Kayhan, Mujde Akturk
- Abdullah Sezer, Gulsum Kayhan, Tugba Ramasli Gursoy, Tugba Sismanlar Eyuboglu, Ferda E Percin