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pro vyhledávání: '"Filiz Azar Aktürk"'
Autor:
Yusuf Gedik, Filiz Azar Aktürk, Halit Reşit Gümele, Emelgül Okur, Ayşenur Ökten, Gülay Karagüzel
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disease. CCD is caused by mutation in the gene on 6p21 encoding transcription factor CBFA1, i.e. runt−related transcription factor 2(RUNX2). The disease is characterized by a persi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e016a21e96f103fc84dbf6e29d62dca
https://pubmed.ncbi.nlm.nih.gov/21274329
https://pubmed.ncbi.nlm.nih.gov/21274329
