Výsledky vyhledávání - "Guler, Hazal Sezginer"

Akademický článek

Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss.

Autor: Zhuri, Drenushe¹ drenushazhuriii@gmail.com, Guler, Hazal Sezginer¹, Yalcintepe, Sinem¹, Demir, Selma¹, Atli, Engin¹, Atli, Emine Ikbal¹, Gurkan, Hakan¹

Publikováno v: Journal of International Advanced Otology. Jul2024, Vol. 20 Issue 4, p312-324. 13p.

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.

Autor: Yalcintepe S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Karal Y; Department of Pediatric Neurology, Faculty of Medicine, Trakya University, Edirne, Turkey., Demir S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Atli EI; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Eker D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Mail C; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Zhuri D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Guler HS; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.

Publikováno v: Global medical genetics [Glob Med Genet] 2023 Jun 16; Vol. 10 (2), pp. 117-122. Date of Electronic Publication: 2023 Jun 16 (Print Publication: 2023).

Zobrazit plný text záznamu

Akademický článek

Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma.

Autor: Yalcintepe S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Korkmaz FN; Department of Endocrinology and Metabolism, Faculty of Medicine, Ankara University, Ankara, Turkey., Demir S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Eker D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Guler HS; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Zhuri D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Atli EI; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Salt SA; Division of Endocrinology, Department of Internal Medicine, Faculty of Medicine, Trakya University, Edirne, Turkey., Sahin M; Department of Endocrinology and Metabolism, Faculty of Medicine, Ankara University, Ankara, Turkey., Guldiken S; Division of Endocrinology, Department of Internal Medicine, Faculty of Medicine, Trakya University, Edirne, Turkey.

Publikováno v: Journal of kidney cancer and VHL [J Kidney Cancer VHL] 2021 Mar 13; Vol. 8 (1), pp. 19-24. Date of Electronic Publication: 2021 Mar 13 (Print Publication: 2021).

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání