Perçin FE - Search Results

1

Aetiological Evaluation of Oligodontia in a Three-Generation Family.

Ergün SG, Tuncer BB, Ergün MA, Kolbaşı G, Orhan M, Perçin FE. Ergün SG, et al. Among authors: percin fe. Oral Health Prev Dent. 2020 Jul 4;18(2):271-275. doi: 10.3290/j.ohpd.a44033. Oral Health Prev Dent. 2020. PMID: 32618450

2

Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome.

Kayhan G, Ergun MA, Ergun SG, Kula S, Percin FE. Kayhan G, et al. Among authors: percin fe. Genet Test Mol Biomarkers. 2018 Aug;22(8):474-480. doi: 10.1089/gtmb.2017.0286. Epub 2018 Jul 26. Genet Test Mol Biomarkers. 2018. PMID: 30048161

3

Evaluation of GenoFlow Thrombophilia Array Test Kit in its detection of mutations in Factor V Leiden (G1691A), prothrombin G20210A, MTHFR C677T and A1298C in blood samples from 113 Turkish female patients.

Aytekin E, Ergun SG, Ergun MA, Percin FE. Aytekin E, et al. Among authors: percin fe. Genet Test Mol Biomarkers. 2014 Nov;18(11):717-21. doi: 10.1089/gtmb.2014.0143. Epub 2014 Aug 25. Genet Test Mol Biomarkers. 2014. PMID: 25153695 Free PMC article.

4

Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by Whole-Exome Sequencing and Homozygosity Mapping.

Sezer A, Kayhan G, Koç A, Ergün MA, Perçin FE. Sezer A, et al. Among authors: percin fe. Cytogenet Genome Res. 2020;160(6):309-315. doi: 10.1159/000509214. Epub 2020 Jun 27. Cytogenet Genome Res. 2020. PMID: 32599602

5

Genome-wide association and whole exome sequencing studies reveal a novel candidate locus for restless legs syndrome.

Ergun U, Say B, Ergun SG, Percin FE, Inan L, Kaygisiz S, Asal PG, Yurteri B, Struchalin M, Shtokalo D, Ergun MA. Ergun U, et al. Among authors: percin fe. Eur J Med Genet. 2021 Apr;64(4):104186. doi: 10.1016/j.ejmg.2021.104186. Epub 2021 Mar 2. Eur J Med Genet. 2021. PMID: 33662638

6

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: percin fe. 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.

7

Investigation of CYP2D6 Gene Polymorphisms in Turkish Population.

Taskin B, Percin FE, Ergun MA. Taskin B, et al. Among authors: percin fe. Psychopharmacol Bull. 2016 Mar 1;46(1):67-72. Psychopharmacol Bull. 2016. PMID: 27738374 Free PMC article.

8

Fibrillin-1 gene intron 56 polymorphism in Turkish children with mitral valve prolapse.

Ozdemir O, Olgunturk R, Karaer K, Ergun MA, Tunaoglu FS, Kula S, Percin FE. Ozdemir O, et al. Among authors: percin fe. Cardiol Young. 2010 Apr;20(2):173-7. doi: 10.1017/S1047951109991284. Epub 2010 Mar 4. Cardiol Young. 2010. PMID: 20199707

9

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. Among authors: percin fe. 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.

10

Identification of copy number variants in children and adolescents with autism spectrum disorder: a study from Turkey.

Özaslan A, Kayhan G, İşeri E, Ergün MA, Güney E, Perçin FE. Özaslan A, et al. Among authors: percin fe. Mol Biol Rep. 2021 Nov;48(11):7371-7378. doi: 10.1007/s11033-021-06745-8. Epub 2021 Oct 12. Mol Biol Rep. 2021. PMID: 34637094

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

45 results

Search Page

Filters