Tuncez E - Search Results

1

Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion.

Zamani AG, Acar A, Durakbasi-Dursun G, Yildirim MS, Ceylaner S, Tuncez E. Zamani AG, et al. Among authors: tuncez e. Am J Med Genet A. 2014 May;164A(5):1239-44. doi: 10.1002/ajmg.a.36410. Epub 2014 Jan 29. Am J Med Genet A. 2014. PMID: 24478222

2

Genetic evaluation of an infertile male with a ring Y chromosome and SHOX deletion.

Zamani AG, Tuncez E, Yildirim MS, Acar A. Zamani AG, et al. Among authors: tuncez e. Genet Couns. 2013;24(4):449-54. Genet Couns. 2013. PMID: 24551992 No abstract available.

3

Micronuclei frequencies in lymphocytes and cervical cells of women with polycystic ovarian syndrome.

Karataylı R, Gül Zamani A, Gezginç K, Tuncez E, Soysal S, Karanfil F, Acar A, Yıldırım MS. Karataylı R, et al. Among authors: tuncez e. Turk J Obstet Gynecol. 2017 Sep;14(3):151-155. doi: 10.4274/tjod.10734. Epub 2017 Sep 30. Turk J Obstet Gynecol. 2017. PMID: 29085703 Free PMC article.

4

Analysis of genetic polymorphisms associated with intervertebral disc degeneration.

Kitis S, Coskun ZM, Tasdemir P, Tuncez E, Zamani AG, Acar A. Kitis S, et al. Among authors: tuncez e. Cell Mol Biol (Noisy-le-grand). 2018 Jul 30;64(10):61-65. Cell Mol Biol (Noisy-le-grand). 2018. PMID: 30084796

5

A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene.

Yıldırım M, Bektaş Ö, Tunçez E, Yeniay Süt N, Sayar Y, Öncül Ü, Teber S. Yıldırım M, et al. Among authors: tuncez e. Mol Syndromol. 2022 Feb;13(2):139-145. doi: 10.1159/000518373. Epub 2021 Sep 30. Mol Syndromol. 2022. PMID: 35418828 Free PMC article.

6

Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey.

Gumus E, Tuncez E, Oz O, Saka Guvenc M. Gumus E, et al. Among authors: tuncez e. Ann Hum Genet. 2021 Jan;85(1):27-36. doi: 10.1111/ahg.12401. Epub 2020 Jul 20. Ann Hum Genet. 2021. PMID: 32686083

7

Peutz-Jeghers Syndrome: A Very Rare Cause of Iron Deficiency Anemia.

Demir Yenigürbüz F, Deveci U, Tuncez E. Demir Yenigürbüz F, et al. Among authors: tuncez e. Turk J Haematol. 2019 Feb 7;36(1):50-51. doi: 10.4274/tjh.galenos.2018.2018.0164. Epub 2018 Jul 24. Turk J Haematol. 2019. PMID: 30040067 Free PMC article. No abstract available.

8

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: tuncez e. Anatol J Cardiol. 2022 Feb;26(2):133-140. doi: 10.5152/AnatolJCardiol.2021.502. Anatol J Cardiol. 2022. PMID: 35190362 Free PMC article.

9

A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia.

Polat R, Ustyol A, Tuncez E, Guran T. Polat R, et al. Among authors: tuncez e. J Endocrinol Invest. 2020 Feb;43(2):185-196. doi: 10.1007/s40618-019-01099-2. Epub 2019 Aug 21. J Endocrinol Invest. 2020. PMID: 31435881

10

Response to Letter to the Editor: "Atrioventricular canal defect is an infrequent congenital heart disease that can be observed in Bardet-Biedl syndrome".

Gumus E, Tuncez E, Oz O, Guvenc MS. Gumus E, et al. Among authors: tuncez e. Ann Hum Genet. 2021 May;85(3-4):103-104. doi: 10.1111/ahg.12420. Epub 2021 Apr 5. Ann Hum Genet. 2021. PMID: 33817793 No abstract available.

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