Get started
Author

Fahrettin Duymus

Observed names: Duymus, Fahrettin, FAHRETTİN DUYMUŞ, Fahrettin Duymuş
Institution: Usak University
ORCID: 0000-0002-8130-9792
Observed ORCID: 0000-0002-8130-9792
OpenAlex ID: A5003550782
Novel Variants in PTPN11 , NF1 , RASA2 , and MAP2K1 : Expanding the Molecular Spectrum of RASopathies in a Turkish Cohort
2026 · Hatice Kocak Eker, Tugba Akın Duman, et al. · Clinical Genetics
Biomarkers for Predicting Immunotherapy Efficacy
2024 · FAHRETTİN DUYMUŞ, TAHA BAHSİ · Turkiye Klinikleri eBooks
Molecular Dynamics Simulation of KIT Mutation in a Patient wıth Piebaldism, Congenital Cataract and Aphakic Glaucoma
2023 · Fahrettin Duymus, Banu Bozkurt, et al. · Journal of Biochemical and Clinical Genetics
A Turkish consanguineous family with a novel stop-gain mutation in SPTBN2 gene leads to spinocerebellar ataxia 14
2021 · Fahrettin Duymus, Ebru Marzioglu Ozdemir, et al. · Molecular Genetics and Metabolism
A novel homozygous PGAP2 mutation causing hyperphosphatasia with mental retardation syndrome-3
2021 · Deniz Esin, Fahrettin Duymus, et al. · Molecular Genetics and Metabolism
Case report: A novel deletion in the NLRP7 gene in the genetic etiology of recurrent hydatidiform mole pregnancy
2021 · Busra Goksel Tulgar, Deniz Esin, et al. · Molecular Genetics and Metabolism
Homozygous LNPK gene mutation in neurodevelopmental disorder: case report
2021 · Fahrettin Duymus, Busra Goksel Tulgar, et al. · Molecular Genetics and Metabolism
Case report: 10q26 deletion syndrome
2021 · Deniz Esin, Fahrettin Duymus, et al. · Molecular Genetics and Metabolism
Neonatal dönemde tanı alan ivemark sendromu vakası: İvemark sendromu
2021 · Duymus, Fahrettin, Sert, Ahmet, et al. · Chronicles of Precision Medical Researchers
PDF
Kromozom 22q11.2 Delesyon Sendromunun Ender Bir Bulgusu: Multikistik Displastik Böbrek
2019 · Fuat Buğrul, Fahrettin Duymuş · Çocuk Dergisi / Journal of Child
PDF
A Case Report of Neurofibromatosis Type 1 Diagnosed with a Noval Mutation Detection in NF1 Gene
2019 · Nafiz Yasa, Busra Eser Cavdartepe, et al. · Selçuk Tıp Dergisi
Works count: 11
Citation count:
H-index:
I10-index:
Year
Topic
Type