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Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.
Eur J Pediatr. 2024 Mar;183(3):1341-1351. doi: 10.1007/s00431-023-05376-4. Epub 2023 Dec 23.
Eur J Pediatr. 2024.
PMID: 38141137
Contribution of Inherited Variants to Hereditary Cancer Syndrome Predisposition.
Güleç Ceylan G, Arslan Satılmış SB, Çavdarlı B, Semerci Gündüz CN.
Güleç Ceylan G, et al.
Tohoku J Exp Med. 2022 Nov 22;258(4):319-325. doi: 10.1620/tjem.2022.J087. Epub 2022 Oct 27.
Tohoku J Exp Med. 2022.
PMID: 36288950
Free article.
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Are angiotensin converting enzyme (ACE1/ACE2) gene variants associated with the clinical severity of COVID-19 pneumonia? A single-center cohort study.
Baştuğ S, Çavdarlı B, Baştuğ A, Şencan İ, Tunçez E, Yakışık Çakır E, Kemirtlek N, Sakar C, Erdem D, Güleç Ceylan G, Özkoçak Turan I, Kazancıoğlu S, Bodur H.
Baştuğ S, et al. Among authors: gulec ceylan g.
Anatol J Cardiol. 2022 Feb;26(2):133-140. doi: 10.5152/AnatolJCardiol.2021.502.
Anatol J Cardiol. 2022.
PMID: 35190362
Free PMC article.
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Clinical and Demographic Characteristics of Cutaneous Mastocytosis in Childhood: Single-center Experience.
Yazal Erdem A, Özyörük D, Emir S, Çakmakçi S, Güleç Ceylan G, Toyran M, Civelek E, Dibek Misirlioğlu E.
Yazal Erdem A, et al. Among authors: gulec ceylan g.
J Pediatr Hematol Oncol. 2022 Jan 1;44(1):e227-e232. doi: 10.1097/MPH.0000000000002196.
J Pediatr Hematol Oncol. 2022.
PMID: 34001789
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A Rare Case of Hanhart Syndrome with Mild Developmental Delay.
Gulec Ceylan G, Tos T, Sari E.
Gulec Ceylan G, et al.
Genet Couns. 2016;27(2):219-22.
Genet Couns. 2016.
PMID: 29485825
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