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Ferda Perçin

4PUBLICATIONS

21CO-AUTHORS

Anthropological geneticsEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseFoetal development and medicine

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Publications (4)

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|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

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Frequent Collaborators

1 joint publications

Tarik Duzenli

1 joint publications

Abdullah Sezer

1 joint publications

Erkan Yurtcu

1 joint publications

Deniz Karçaaltıncaba

1 joint publications

Hasan Hüseyin Kazan

1 joint publications

Halis Özdemir

1 joint publications

Meral Yirmibeş Karaoğuz

1 joint publications

Pinar Çalış

1 joint publications

Gülsüm Kayhan

1 joint publications

Sezen Güntekin Ergün

Frequent Collaborators

1 joint publications

Tarik Duzenli

1 joint publications

Abdullah Sezer

1 joint publications

Erkan Yurtcu

1 joint publications

Deniz Karçaaltıncaba

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