Tuğ E - Search Results

1

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses.

Tuğ E, Karcaaltincaba D, Yirmibeş Karaoğuz M, Saat H, Özek A. Tuğ E, et al. J Matern Fetal Neonatal Med. 2017 Jul;30(13):1579-1583. doi: 10.1080/14767058.2016.1214700. Epub 2016 Oct 26. J Matern Fetal Neonatal Med. 2017. PMID: 27431726 Free article.

2

Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion.

Kayhan G, Calis P, Karcaaltincaba D, Tug E. Kayhan G, et al. Among authors: tug e. J Obstet Gynaecol. 2019 Nov;39(8):1175-1176. doi: 10.1080/01443615.2019.1601165. Epub 2019 Jun 24. J Obstet Gynaecol. 2019. PMID: 31234679 Free article. No abstract available.

3

Expression of the syncytin-1 and syncytin-2 genes in the trophoblastic tissue of the early pregnancy losses with normal and abnormal karyotypes.

Tug E, Yirmibes Karaoguz M, Nas T. Tug E, et al. Gene. 2020 May 30;741:144533. doi: 10.1016/j.gene.2020.144533. Epub 2020 Mar 4. Gene. 2020. PMID: 32145327

4

Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.

Tuğ E, Yirmibeş Karaoğuz M, Kayhan G, Ergün MA, Perçin FE. Tuğ E, et al. Am J Med Genet A. 2014 Jul;164A(7):1770-6. doi: 10.1002/ajmg.a.36495. Epub 2014 Mar 26. Am J Med Genet A. 2014. PMID: 24677787 Review.

5

Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing.

Bakır A, Yirmibeş Karaoğuz M, Perçin FE, Tuğ E, Cinaz P, Ergün MA. Bakır A, et al. Among authors: tug e. Turk J Med Sci. 2018 Apr 30;48(2):386-390. doi: 10.3906/sag-1711-74. Turk J Med Sci. 2018. PMID: 29714459 Free article.

6

Interleukin-10 gene promoter polymorphism in patients with schizophrenia in a region of East Turkey.

Ozbey U, Tug E, Namli M. Ozbey U, et al. Among authors: tug e. World J Biol Psychiatry. 2009;10(4 Pt 2):461-8. doi: 10.1080/15622970802626580. World J Biol Psychiatry. 2009. PMID: 19153889

7

A patient with 9q subtelomeric deletion syndrome with additional findings.

Tug E, Cavdarli B, Karaoguz MY, Percin FE. Tug E, et al. Genet Couns. 2012;23(4):465-71. Genet Couns. 2012. PMID: 23431745

8

Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region.

Tuğ E, Ergün MA, Perçin EF. Tuğ E, et al. Turk J Pediatr. 2018;60(1):94-98. doi: 10.24953/turkjped.2018.01.015. Turk J Pediatr. 2018. PMID: 30102487 Free article.

9

A Turkish family with Nance-Horan Syndrome due to a novel mutation.

Tug E, Dilek NF, Javadiyan S, Burdon KP, Percin FE. Tug E, et al. Gene. 2013 Aug 1;525(1):141-5. doi: 10.1016/j.gene.2013.03.094. Epub 2013 Apr 6. Gene. 2013. PMID: 23566852

10

The evaluation of long-term effects of ionizing radiation through measurement of current sister chromatid exchange (SCE) rates in radiology technologists, compared with previous SCE values.

Tug E, Kayhan G, Kan D, Guntekin S, Ergun MA. Tug E, et al. Mutat Res. 2013 Sep 18;757(1):28-30. doi: 10.1016/j.mrgentox.2013.04.025. Epub 2013 Jul 15. Mutat Res. 2013. PMID: 23867852

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