Yayın
101
Açık Erişim
15
Ödüller
3
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Eylül 2022 A cause of familial central precocious puberty: A Novel variant in the DLK1 gene and low serum DLK1 levels, ESPE Travel Grant To Attend The 60Th Annual ESPE Meeting 2022,Rome
Espe And The Programme Organising Committee
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Eylül 2021 Sequence of MKRN3 and DLK1 genes in cases with familial central precocious puberty, ESPE Registration Grant To Attend The 59Th Annual Espe Meeting Online
Espe And The Programme Organising Committee
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Haziran 2020 Two cases with central precocious puberty caused by paternally inherited novel variants in DLK1gene
European Human Genetics Conference 2020