Clinical and phenotypic features of osteogenesis imperfecta caused by fkbp10 mutations: a study of skeletal deformities and cervical abnormalities

Canbaz A. T., GÜNAY A., Kurt I., KELEŞTEMUR E., KAHVECİ A., CANBAZ S. B., ...Daha Fazla

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025:, Danimarka, 10 Mart 2025, (Tam Metin Bildiri)

  • Yayın Türü: Bildiri / Tam Metin Bildiri
  • Basıldığı Ülke: Danimarka
  • Marmara Üniversitesi Adresli: Evet