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Çapan, Özlem Yalçın
23
results:
Search for persons
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Format
Online (23)
Mediatypes
Articles (Online) (11)
OpenAccess-fulltext (12)
Sorted by: Relevance
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1
Developmental and epileptic encephalopathy 82 (DEE82) with ..:
Çapan, Özlem Yalçın
;
Türkdoğan, Dilşad
;
Atalay, Sertaç
.
Seizure: European Journal of Epilepsy. 116 (2024) - p. 126-132 , 2024
Link:
https://doi.org/10.1016/..
?
2
Exome data of developmental and epileptic encephalopathy pa..:
Çapan, Özlem Yalçın
;
Yapıcı, Zuhal
;
Özbil, Mehmet
.
Seizure: European Journal of Epilepsy. 116 (2024) - p. 51-64 , 2024
Link:
https://doi.org/10.1016/..
?
3
HNF1A-MODY Mutations in Nuclear Localization Signal Impair ..:
Fareed, Fareed M. A.
;
Korulu, Sirin
;
Özbil, Mehmet
.
The Protein Journal. 40 (2021) 4 - p. 512-521 , 2021
Link:
https://doi.org/10.1007/..
?
4
De novo 8p23.1 deletion in a patient with absence epilepsy:
Akcakaya, Nihan Hande
;
Capan, Özlem Yalcin
;
Schulz, Herbert
...
Epileptic Disorders. 19 (2017) 2 - p. 217-221 , 2017
Link:
https://doi.org/10.1684/..
?
5
A Common VWF Exon 28 Haplotype in the Turkish Population:
Berber, Ergul
;
Pehlevan, Funda
;
Akin, Mehmet
...
Clinical and Applied Thrombosis/Hemostasis. 19 (2012) 5 - p. 550-556 , 2012
Link:
https://doi.org/10.1177/..
?
6
A Review of Functional Characterization of Single Amino Aci..:
Çubuk, Hasan
;
Yalçın Çapan, Özlem
The Protein Journal. 40 (2021) 3 - p. 348-360 , 2021
Link:
https://doi.org/10.1007/..
?
7
Whole exome sequencing reveals novel candidate gene variant..:
Yalçın Çapan, Özlem
;
Aydın, Neslihan
;
Yılmaz, Temel
.
Clinica Chimica Acta. 510 (2020) - p. 97-104 , 2020
Link:
https://doi.org/10.1016/..
?
8
SCN1A gene sequencing in 46 Turkish epilepsy patients discl..:
Usluer, Sunay
;
Salar, Seda
;
Arslan, Mutluay
...
Seizure. 39 (2016) - p. 34-43 , 2016
Link:
https://doi.org/10.1016/..
?
9
HNF1A-MODY Mutations in Nuclear Localization Signal Impair ..:
Fareed, Fareed M. A
;
Korulu, Sirin
;
Ozbil, Mehmet
.
https://aperta.ulakbim.gov.tr/record/233502. , 2021
Link:
https://aperta.ulakbim.g..
?
10
Whole exome sequencing reveals novel candidate gene variant..:
Capan, Ozlem Yalcin
;
Aydin, Neslihan
;
Yilmaz, Temel
.
https://aperta.ulakbim.gov.tr/record/9193. , 2020
Link:
https://aperta.ulakbim.g..
?
11
Comparison of Crosslinker Types and Initiation Systems of T..:
Hatır, Pınar Çakır
;
Capan, Özlem Yalçın
Düzce Üniversitesi Bilim ve Teknoloji Dergisi. , 2019
Link:
https://doi.org/10.29130..
?
12
De novo 8p23.1 deletion in a patient with absence epilepsy:
Akcakaya, Nihan Hande
;
Capan, Ozlem Yalcin
;
Schulz, Herbert
...
https://aperta.ulakbim.gov.tr/record/44225. , 2017
Link:
https://aperta.ulakbim.g..
?
13
SCN1A gene sequencing in 46 Turkish epilepsy patients discl..:
Usluer, Sunay
;
Salar, Seda
;
Arslan, Mutluay
...
https://aperta.ulakbim.gov.tr/record/60489. , 2016
Link:
https://aperta.ulakbim.g..
?
14
SCN1A gene sequencing in 46 Turkish epilepsy patients discl..:
KARA, BÜLENT
;
Usluer, Sunay
;
Salar, Seda
...
d1c42fc4-090b-4dc4-b776-f0f3046cbaea. , 2016
Link:
https://doi.org/10.1016/..
?
15
Synthesis, Characterization and Biocompatibility Oo Plant-O..:
Yalçın Çapan, Özlem
;
Çakır Hatır, Pınar
Trakya University Journal of Natural Sciences. , 2021
Link:
https://doi.org/10.23902..
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