Bayrakli S - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family group.

Bayrakli F, Guney I, Bayri Y, Ercan-Sencicek AG, Ceyhan D, Cankaya T, Mason C, Bilguvar K, Bayrakli S, Mane SM, State MW, Gunel M. Bayrakli F, et al. Among authors: bayrakli s. J Clin Neurosci. 2009 Dec;16(12):1610-4. doi: 10.1016/j.jocn.2009.03.022. Epub 2009 Sep 29. J Clin Neurosci. 2009. PMID: 19793656

Heterozygous 5p13.3-13.2 deletion in a patient with type I Chiari malformation and bilateral Duane retraction syndrome.

Bayrakli F, Bilguvar K, Ceyhan D, Ercan-Sencicek AG, Cankaya T, Bayrakli S, Guney I, Mane SM, State MW, Gunel M. Bayrakli F, et al. Among authors: bayrakli s. Clin Genet. 2010 May;77(5):499-502. doi: 10.1111/j.1399-0004.2010.01411.x. Clin Genet. 2010. PMID: 20447154 No abstract available.

Reduced coronary flow reserve and early diastolic filling abnormalities in patients with nephrotic syndrome.

Oflaz H, Sen F, Bayrakli SK, Elitok A, Cimen AO, Golcuk E, Kasikcioglu E, Tukenmez M, Yazici H, Turkmen A. Oflaz H, et al. Among authors: bayrakli sk. Ren Fail. 2008;30(9):914-20. doi: 10.1080/08860220802353819. Ren Fail. 2008. PMID: 18925532 Free article.

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

3 results

Search Page

Filters