Hanife Saat
5PUBLICATIONS
22CO-AUTHORS
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Publications (5)
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|Jul 04, 2025
A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia.Abdullah Sezer, Sukru S Oner, Hanife Saat
|Apr 07, 2025
Multilocus Disease-Causing Genomic Variations for Genetic Disorders: Single Tertiary Centre Experience From Türkiye.Ahmet Kablan, Abdullah Sezer, Abdullatif Bakır
|Jun 23, 2022
Genetic Etiology of Ichthyosis in Turkish Patients: Next-generation Sequencing Identified Seven Novel MutationsHanife Saat, Ibrahim Sahin, Neslihan Duzkale
|Jan 28, 2022
New Perspectives on the Recurrent Monoallelic Germline Mutations of DNA Repair and Checkpoint Genes and Clinical Variability.Ibrahim Sahin, Hanife Saat
|Jun 19, 2021
A novel BRCA1 duplication and new insights on the spectrum and frequency of germline large genomic rearrangements in BRCA1/BRCA2.Ibrahim Sahin, Hanife Saat
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Frequent Collaborators
3 joint publications
Ibrahim Sahin
2 joint publications
Abdullah Sezer
1 joint publications
Neslihan Duzkale
1 joint publications
Muzeyyen Gonul
1 joint publications
Taha Bahsi
1 joint publications
Ahmet Kablan
1 joint publications
Abdullatif Bakır
1 joint publications
Elifcan Taşdelen
1 joint publications
Firdevs Dinçsoy Bir
1 joint publications
Haktan Bagis Erdem
