Ferda Perçin

4PUBLICATIONS
21CO-AUTHORS
Anthropological geneticsEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseFoetal development and medicine
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (4)

|Mar 17, 2025
Clinical and Molecular Analyses in 8 New Craniofrontonasal Syndrome Families: Revisiting the Mild End of the Phenotypic Spectrum in Females.

Umut Altunoglu, Birsen Karaman, Yasemin Alanay

|Dec 16, 2023
Letter 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.

Tarik Duzenli, Abdullah Sezer, Ferda Emriye Percin

|Jun 16, 2022
Pitt-Hopkins syndrome accompanying hypoxic ischemic encephalopathy in a newborn.

Melda Tas, Mervenur Kurtulus, Elı F Keles Gulnerman

|Dec 14, 2020
Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies?

Erkan Yurtcu, Deniz Karçaaltıncaba, Hasan Hüseyin Kazan

Pageof 1

Frequent Collaborators

1 joint publications

Tarik Duzenli

1 joint publications

Abdullah Sezer

1 joint publications

Erkan Yurtcu

1 joint publications

Deniz Karçaaltıncaba