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Canan Ceylan Kose

3PUBLICATIONS

13CO-AUTHORS

Gene mappingCell and nuclear divisionDevelopmental genetics (incl. sex determination)

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Publications (3)

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|Oct 11, 2024

Spinal muscular atrophy carrier screening program: awareness and attitude of healthcare professionals in Turkey.

Kubra Muge Celik, Canan Ceylan Kose, Derya Kaya

|Aug 21, 2024

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow.

Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano

|May 16, 2023

Anemia and thrombocytopenia due to a novel BRPF1 variant in a family from Çanakkale with intellectual disability and dysmorphic facies: Case report and review of the literature.

Canan Ceylan Kose, Derya Kaya, Mehmet Berkay Akcan

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Frequent Collaborators

2 joint publications

Derya Kaya

2 joint publications

Fatma Silan

1 joint publications

Mehmet Berkay Akcan

1 joint publications

Angelina Haesoo Kim

1 joint publications

Irmak Sakin

1 joint publications

Stephen Viviano

1 joint publications

Sukru Sadik Oner

1 joint publications

Oktay I Kaplan

1 joint publications

Mahmut Cerkez Ergoren

1 joint publications

Sehime G Temel

Frequent Collaborators

2 joint publications

Derya Kaya

2 joint publications

Fatma Silan

1 joint publications

Mehmet Berkay Akcan

1 joint publications

Angelina Haesoo Kim

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