Ferda Emriye Percin (Ferda Percin, Ferda Perçin)
Publication Activity (10 Years)
Years Active: 2021-2023
Publications (10 Years): 6
Publications (10 Years): 6
Publications
- 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)
- 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)
- Melda Tas, Mervenur Kurtulus, Elı F Keles Gulnerman, Canan Turkyilmaz, Ferda Emriye Percin, Ebru Ergenekon, Esin Koc