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Ali Topak

Showing results (1-10 of 20) with videos related to

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Laboratory Medicine|April 20, 2023
Molecular diagnostic results of a nephropathy gene panel in patients with suspected hereditary kidney diseaseAli Topak
Clinical Dysmorphology|July 9, 2020
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature reviewMehmet Bugrahan Duz, Ali Topak
American Journal of Medical Genetics. Part A|March 25, 2023
Clinical exome sequencing findings in 1589 patientsOzlem Gorukmez, Orhan Gorukmez, Ali Topak
Human Heredity|February 13, 2025
RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in TurkeyOrhan Gorukmez, Ozlem Gorukmez, Ali Topak
Fetal and Pediatric Pathology|September 22, 2023
ATP7B Gene Variant Profile İdentified by NGS in Wilson's DiseaseOrhan Gorukmez, Taner Özgür, Ozlem Gorukmez, et al.
Cureus|April 10, 2025
Clinical Exome Sequencing in Pediatric PatientsOrhan Görükmez, Özlem Görükmez, Ali Topak, et al.
Neurological Research|May 26, 2021
Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutationsCengiz Havali, Arzu Ekici, Sevil Dorum, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 11, 2021
Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variantsSevil Dorum, Hakan Erdoğan, Adem Yasin Köksoy, et al.
European Journal of Ophthalmology|January 21, 2025
H syndrome with bilateral choroidal osteoma: Coincidence or association?Ayna Sariyeva Ismayilov, Derya Doğanay, Mahmut Oğuz Ulusoy, et al.
Clinical Rheumatology|January 9, 2015
Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel syndromePınar Eroğlu, Esra Erkol İnal, Şebnem Özemri Sağ, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Laboratory Medicine|April 20, 2023
Molecular diagnostic results of a nephropathy gene panel in patients with suspected hereditary kidney diseaseAli Topak
Clinical Dysmorphology|July 9, 2020
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature reviewMehmet Bugrahan Duz, Ali Topak
American Journal of Medical Genetics. Part A|March 25, 2023
Clinical exome sequencing findings in 1589 patientsOzlem Gorukmez, Orhan Gorukmez, Ali Topak
Human Heredity|February 13, 2025
RNA-Based Next-Generation Sequencing Approach to Non-Small Cell Lung Cancer: A Single-Center Experience in TurkeyOrhan Gorukmez, Ozlem Gorukmez, Ali Topak
Fetal and Pediatric Pathology|September 22, 2023
ATP7B Gene Variant Profile İdentified by NGS in Wilson's DiseaseOrhan Gorukmez, Taner Özgür, Ozlem Gorukmez, et al.
Cureus|April 10, 2025
Clinical Exome Sequencing in Pediatric PatientsOrhan Görükmez, Özlem Görükmez, Ali Topak, et al.
Neurological Research|May 26, 2021
Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutationsCengiz Havali, Arzu Ekici, Sevil Dorum, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 11, 2021
Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variantsSevil Dorum, Hakan Erdoğan, Adem Yasin Köksoy, et al.
European Journal of Ophthalmology|January 21, 2025
H syndrome with bilateral choroidal osteoma: Coincidence or association?Ayna Sariyeva Ismayilov, Derya Doğanay, Mahmut Oğuz Ulusoy, et al.
Clinical Rheumatology|January 9, 2015
Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel syndromePınar Eroğlu, Esra Erkol İnal, Şebnem Özemri Sağ, et al.
Pageof 2