SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects | Nature Communications
DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune–Albright syndrome and cutaneous skeletal hypophosphatemia syndrome in: European Journal of Endocrinology Volume 182 Issue 5 (2020)
Applied Sciences | Free Full-Text | Personalized Bone Reconstruction and Regeneration in the Treatment of Craniosynostosis | HTML
Surgical Removal of Fibrous Dysplasia From the Craniofacial Skeleton | Plastic Surgery Key
Fibrous dysplasia of bone: craniofacial and dental implications - Burke - 2017 - Oral Diseases - Wiley Online Library
Skeletal Dysplasias - Endotext - NCBI Bookshelf
Clinical guidelines for the management of craniofacial fibrous dysplasia | Orphanet Journal of Rare Diseases | Full Text
Positive Association between Fibrous Dysplasia (FD) related 18F-NaF activity and Bone Turnover Markers (BTMs). | Journal of Nuclear Medicine
Genetic Disorders and Bone Affecting the Craniofacial Skeleton - Oral and Maxillofacial Surgery Clinics
Markers for specific skeletal stem cell populations. a In long bones,... | Download Scientific Diagram
Sclerosing bone dysplasias with involvement of the craniofacial skeleton - ScienceDirect
Craniofacial bone and cartilage abnormalities in clcn7 morphants. (A)... | Download Scientific Diagram
18F‐NaF PET/CT IMAGING IN FIBROUS DYSPLASIA OF BONE - Papadakis - 2019 - Journal of Bone and Mineral Research - Wiley Online Library
Frontiers | Bone Phenotyping Approaches in Human, Mice and Zebrafish – Expert Overview of the EU Cost Action GEMSTONE (“GEnomics of MusculoSkeletal traits TranslatiOnal NEtwork”) | Endocrinology
Comprehensive management of malocclusion in maxillary fibrous dysplasia: A case report
A skeletal survey of the patient. (A, B) The craniofacial bones show... | Download Scientific Diagram
Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss | Scientific Reports
Fgfr3 mutation disrupts chondrogenesis and bone ossification in zebrafish model mimicking CATSHL syndrome partially via enhanced Wnt/β-catenin signaling
Advances in bone dysplasias | Revista Española de Cirugía Ortopédica y Traumatología (English Edition)
PDF) Bone markers in craniofacial bone deformations and dysplasias
STAT3 is critical for skeletal development and bone homeostasis by regulating osteogenesis | Nature Communications
Representative radiographic features of fibrous dysplasia. a Femoral... | Download Scientific Diagram
Frontiers | Advances in Models of Fibrous Dysplasia/McCune-Albright Syndrome | Endocrinology
