Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Seref Tuncer"'
Autor:
Demet Akdeniz Odemis, Rejin Kebudi, Seda Kilic Erciyas, Gozde Kuru Turkcan, Seref Tuncer, Ozge Sukruoglu Erdogan, Jamila Bayramova, Betul Celik, Busra Kurt Gultaslar, Sema Büyükkapu Bay, Samuray Tuncer, Hülya Yazici
The aim of the study was to investigate the frequency and types of mutations on the RB1 gene at the familial, clinical, and ethnic levels which are known to have an important role in the genetics of retinoblastoma in Turkish population. RB1 gene muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6920434696cc1db5806c18b185cb303
https://doi.org/10.22541/au.164878743.32929207/v1
https://doi.org/10.22541/au.164878743.32929207/v1
Autor:
Rejin Kebudi, Demet Akdeniz, Jamila Bayramova, Seda Kilic Erciyas, Gozde Kuru Turkcan, Bugra Seref Tuncer, Ozge Sukruoglu, Betul Celik, Busra Kurt Gultaslar, Sema Bay Buyukkapu, Samuray Tuncer, Hulya Yazici
Publikováno v:
Journal of Clinical Oncology. 40:e22007-e22007
e22007 Background: Retinoblastoma (RB) is the most common intraocular malignancy in children, caused by mutations in the tumor suppressor RB1 gene. Patients with bilateral/trilateral/familial RB are considered to have hereditary RB (1 germline, 1 som
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd41fd419cded8510d1e9892fe65e16b
https://doi.org/10.1200/jco.2022.40.16_suppl.e22007
https://doi.org/10.1200/jco.2022.40.16_suppl.e22007
