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1 . Academic Journal
Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients
저자
by
Ozkalayci, Hande
;
Bora, Elcin
;
Cankaya, Tufan
;
Kocabey, Mehmet
;
Zubari, Nadide Cemre
, et al.
소스
Neurogenetics: New developments in Neurogenetics and Neuroepigenetics.
. 25(3):201-213
Web of Science
Scopus
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7 . Academic Journal
Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Answers
저자
by
Bayram, Meral Torun
;
Yildiz, Gizem
;
Cağlayan, Ahmet Okay
;
Ulgenalp, Ayfer
;
Unlu, Sadiye Mehtat
, et al.
소스
Pediatric Nephrology: Journal of the International Pediatric Nephrology Association
. 38(1):115-117
Web of Science
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7 . Academic Journal
Effects of GLP-1 Receptor Polymorphisms on Adolescent Obesity
저자
by
Mahafarin Maralani
;
Tufan Cankaya
;
Esra Ataman
;
Yavuz Tokgoz
;
Erkan Kaytankas
, et al.
소스
Acta Medica Iranica, Vol 61, Iss 4 (2023)
Open Access (DOAJ)
Scopus
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7 . Academic Journal
MIRAGE syndrome in a 10-year-old girl with a novel Lys1024Glu missense variant in SAMD9
저자
by
Cinleti, Tayfun
;
Gülen, Ali
;
Sönmez, Beria
;
Gürsoy, Semra
;
Boyacioğlu, Özge Kangalli
, et al.
소스
Clinical Dysmorphology
. Jul 01, 2023 32(3):133-138
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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
Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey
저자
by
Bora, Elcin
;
Caglayan, Ahmet Okay
;
Koc, Altug
;
Cankaya, Tufan
;
Ozkalayci, Hande
, et al.
소스
In
Cancer Genetics
April 2022 262-263:118-133
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7 . Academic Journal
Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Questions
저자
by
Bayram, Meral Torun
;
Yildiz, Gizem
;
Cağlayan, Ahmet Okay
;
Ulgenalp, Ayfer
;
Unlu, Sadiye Mehtat
, et al.
소스
Pediatric Nephrology: Journal of the International Pediatric Nephrology Association
. 38(1):113-114
Web of Science
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7 . Academic Journal
Spondyloepimetaphyseal dysplasia-Maroteaux type due to dominant TRPV4 mutation: expanding the phenotype with a case report
저자
by
Uzman, Ceren Yılmaz
;
Çankaya, Tufan
;
Güleryüz, Handan
;
Ülgenalp, Ayfer
;
Bozkaya, Özlem Giray
.
소스
Skeletal Radiology: Journal of the International Skeletal Society A Journal of Radiology, Pathology and Orthopedics
. 52(1):115-118
Web of Science
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7 . Academic Journal
Cinsiyet Disforisinde Genetik Faktörlerin Rolü
저자
by
Duygu Onur Cura
;
Ayfer Ulgenalp
;
Tufan Çankaya
.
소스
Hitit Medical Journal, Vol 2, Iss 2, Pp 49-55 (2020)
Open Access (DOAJ)
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5 . Academic Journal
Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy
저자
by
Semra Gursoy
;
Esra Ataman
;
Bahar Toklu Baysal
;
Berk Özyılmaz
;
Pınar Gençpınar
, et al.
소스
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 206-210 (2020)
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