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1 . Academic Journal
Interstitial 3p25.3 deletion syndrome: 13 years’-long follow-up of an affected individual
저자
by
Kocagil, Sinem
;
Susam, Ezgi
;
Yimenicioğlu, Sevgi
;
Aynaci, Sabri
;
Gökalp, Ebru Erzurumluoğlu
, et al.
소스
Clinical Dysmorphology
. May 21, 2024
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7 . Academic Journal
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
저자
by
Dundar, Munis
;
Fahrioglu, Umut
;
Yildiz, Saliha Handan
;
Bakir-Gungor, Burcu
;
Temel, Sehime Gulsun
, et al.
소스
Functional & Integrative Genomics
. 22(3):291-315
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7 . Academic Journal
A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay
저자
by
Samanci, Bedia
;
Gokalp, Ebru Erzurumluoglu
;
Bilgic, Basar
;
Gurvit, Hakan
;
Artan, Sevilhan
, et al.
소스
Neurological Sciences
. 42(7):2969-2973
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7 . Academic Journal
Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey
저자
by
Nadir Unlu
;
Ebru Erzurumluoglu Gokalp
;
Serap Arslan
;
Oguz Cilingir
;
Muzaffer Bilgin
, et al.
소스
International Journal of Ophthalmology, Vol 14, Iss 6, Pp 812-817 (2021)
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7 . Academic Journal
A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease
저자
by
Guven, Gamze
;
Samanci, Bedia
;
Gulec, Cagri
;
Hanagasi, Hasmet
;
Gurvit, Hakan
, et al.
소스
Neurological Sciences
. 42(6):2497-2504
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7 . Academic Journal
Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?
저자
by
Beyhan Durak Aras
;
Sevgi Isik
;
Hava Uskudar Teke
;
Abdulvahap Aslan
;
Filiz Yavasoglu
, et al.
소스
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
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7 . Academic Journal
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients
저자
by
Taner Ulus
;
Muhammet Dural
;
Pelin Meşe
;
Furkan Yetmiş
;
Kadir Uğur Mert
, et al.
소스
Anatolian Journal of Cardiology, Vol 25, Iss 2, Pp 129-138 (2021)
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7 . Academic Journal
Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus
저자
by
Enver Şimşek
;
Oğuz Çilingir
;
Tülay Şimşek
;
Sinem Kocagil
;
Ebru Erzurumluoğlu Gökalp
, et al.
소스
JCRPE, Vol 16, Iss 2, Pp 137-145 (2024)
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7 . Academic Journal
Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?
저자
by
Durak Aras, Beyhan
;
Isik, Sevgi
;
Uskudar Teke, Hava
;
Aslan, Abdulvahap
;
Yavasoglu, Filiz
, et al.
소스
Molecular Cytogenetics
. 14(1)
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7 . Academic Journal
Frequency of frontotemporal dementia-related gene variants in Turkey
저자
by
Artan, Sevilhan
;
Erzurumluoglu Gokalp, Ebru
;
Samanci, Bedia
;
Ozbabalik Adapinar, Demet
;
Bas, Hasan
, et al.
소스
In
Neurobiology of Aging
October 2021 106:332-332
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