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Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort.
Aydin, Hatip; Gunay, Murat; Celik, Gokhan; Gunay, Betul Onal; Aydin, Umeyye Taka; Karaman, Ali.
Affiliation
  • Aydin H; a Center of Genetics Diagnosis, Zeynep Kamil Maternity and Children's Disease Training and Research Hospital , Istanbul , Turkey.
  • Gunay M; b Department of Ophthalmology, ROP Screening , Treatment and Training Center, Zeynep Kamil Maternity and Children's Disease Training and Research Hospital , Istanbul , Turkey.
  • Celik G; b Department of Ophthalmology, ROP Screening , Treatment and Training Center, Zeynep Kamil Maternity and Children's Disease Training and Research Hospital , Istanbul , Turkey.
  • Gunay BO; c Department of Ophthalmology , Umraniye Training and Research Hospital , Istanbul , Turkey.
  • Aydin UT; d Department of Ophthalmology, Tuzla State Hospital , Istanbul , Turkey.
  • Karaman A; a Center of Genetics Diagnosis, Zeynep Kamil Maternity and Children's Disease Training and Research Hospital , Istanbul , Turkey.
Ophthalmic Genet ; 37(4): 415-418, 2016 12.
Article in En | MEDLINE | ID: mdl-27018927
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Database: MEDLINE Main subject: Retinopathy of Prematurity / Factor V / Prothrombin / Polymorphism, Single Nucleotide / Methylenetetrahydrofolate Reductase (NADPH2) Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2016 Type: Article Affiliation country: Turkey
Search on Google
Add to My VHL
Print
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PubMed Links

Database: MEDLINE Main subject: Retinopathy of Prematurity / Factor V / Prothrombin / Polymorphism, Single Nucleotide / Methylenetetrahydrofolate Reductase (NADPH2) Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2016 Type: Article Affiliation country: Turkey