Yıldırım MS - Search Results

1

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.

Erdoğan M, Köse M, Pekcan S, Hangül M, Balta B, Kiraz A, Akıncı Gönen G, Zamani AG, Yıldırım MS, Ramaslı Gürsoy T, Ezgu F, Şişmanlar Eyüpoğlu T, Tana Aslan A. Erdoğan M, et al. Among authors: yildirim ms. Balkan Med J. 2021 Nov;38(6):357-364. doi: 10.5152/balkanmedj.2021.21199. Balkan Med J. 2021. PMID: 34860163 Free PMC article.

2

Spectrum of mutations in the familial Mediterranean fever gene (MEFV) in Turkish patients of the Central Anatolia region: a comparison of two mutation detection system.

Zamani AG, Acar A, Yildirim MS. Zamani AG, et al. Among authors: yildirim ms. Genet Mol Res. 2013 Oct 29;12(4):5152-9. doi: 10.4238/2013.October.29.9. Genet Mol Res. 2013. PMID: 24301775 Free article.

3

K-ras oncogene mutation in pterygium.

Ozturk BT, Yıldırım MS, Zamani A, Bozkurt B. Ozturk BT, et al. Among authors: yildirim ms. Eye (Lond). 2017 Mar;31(3):491-498. doi: 10.1038/eye.2016.254. Epub 2016 Nov 11. Eye (Lond). 2017. PMID: 27834959 Free PMC article. Clinical Trial.

4

Extended-spectrum of KRAS and NRAS mutations in lung cancer tissue specimens obtained with bronchoscopy.

Basdemirci M, Zamani A, Zamani AG, Findik S, Yildirim MS. Basdemirci M, et al. Among authors: yildirim ms. Indian J Cancer. 2022 Apr-Jun;59(2):236-243. doi: 10.4103/ijc.IJC_766_19. Indian J Cancer. 2022. PMID: 34380837 Free article.

5

Warburg micro syndrome in two children from a highly inbred Turkish family.

Yildirim MS, Zamani AG, Bozkurt B. Yildirim MS, et al. Genet Couns. 2012;23(2):169-74. Genet Couns. 2012. PMID: 22876574

6

Effect of mobile phone station on micronucleus frequency and chromosomal aberrations in human blood cells.

Yildirim MS, Yildirim A, Zamani AG, Okudan N. Yildirim MS, et al. Among authors: yildirim a. Genet Couns. 2010;21(2):243-51. Genet Couns. 2010. PMID: 20681227

7

Evaluation of death pathway genes FAS and FASL polymorphisms in chronic HBV infection.

Zamani AG, Barlas IO, Durakbasi-Dursun G, Ural O, Erdal E, Yildirim MS. Zamani AG, et al. Among authors: yildirim ms. Int J Immunogenet. 2013 Dec;40(6):482-7. doi: 10.1111/iji.12056. Epub 2013 Apr 7. Int J Immunogenet. 2013. PMID: 23560484

8

LAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findings.

Basdemirci M, Zamani AG, Sener S, Tassoker M, Cetmili H, Zamani A, Aydogdu D, Basdemirci A, Yildirim MS. Basdemirci M, et al. Among authors: yildirim ms. Clin Dysmorphol. 2019 Apr;28(2):81-85. doi: 10.1097/MCD.0000000000000254. Clin Dysmorphol. 2019. PMID: 30433887 No abstract available.

9

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: yildirim ms. Genet Couns. 2013;24(4):449-54. Genet Couns. 2013. PMID: 24551992 No abstract available.

10

Down syndrome associated with severe combined immunodeficiency: a case report.

Yildirim MS, Artac H, Reisli I. Yildirim MS, et al. Genet Couns. 2009;20(3):269-73. Genet Couns. 2009. PMID: 19852434

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

116 results

Search Page

Filters