Fibrous dysplasia of bone: craniofacial and dental implications - Burke - 2017 - Oral Diseases - Wiley Online Library
A primer on skeletal dysplasias | SpringerLink
Fibrous dysplasia of bone: craniofacial and dental implications - Burke - 2017 - Oral Diseases - Wiley Online Library
Craniofacial bone and cartilage abnormalities in clcn7 morphants. (A)... | Download Scientific Diagram
Applied Sciences | Free Full-Text | Personalized Bone Reconstruction and Regeneration in the Treatment of Craniosynostosis
Advances in bone dysplasias | Revista Española de Cirugía Ortopédica y Traumatología (English Edition)
Fibrous dysplasia of bone: craniofacial and dental implications - Burke - 2017 - Oral Diseases - Wiley Online Library
Markers for specific skeletal stem cell populations. a In long bones,... | Download Scientific Diagram
Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders
Making and shaping endochondral and intramembranous bones - Galea - 2021 - Developmental Dynamics - Wiley Online Library
Skeletal Dysplasias | SpringerLink
Bone fragility in patients affected by congenital diseases non skeletal in origin | Orphanet Journal of Rare Diseases | Full Text
Sclerosing bone dysplasias with involvement of the craniofacial skeleton - ScienceDirect
Skeletal Dysplasias - Endotext - NCBI Bookshelf
Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders
Gαs signaling controls intramembranous ossification during cranial bone development by regulating both Hedgehog and Wnt/β-catenin signaling | Bone Research
![Multicentric Osteolysis, Nodulosis, and Arthropathy in Two Unrelated Children with Matrix Metalloproteinase 2 Variants: Genetic-Skeletal Correlations[v1] | Preprints](https://www.preprints.org/img/dyn_abstract_figures/2021/05/1ec609aa7d3ed4ce4a8aec6a0547a6be/preprints-43519-GA%201200%20px.jpg "Multicentric Osteolysis, Nodulosis, and Arthropathy in Two Unrelated Children with Matrix Metalloproteinase 2 Variants: Genetic-Skeletal Correlations[v1] | Preprints")
Multicentric Osteolysis, Nodulosis, and Arthropathy in Two Unrelated Children with Matrix Metalloproteinase 2 Variants: Genetic-Skeletal Correlations[v1] | Preprints
Frontiers | A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling | Nature Communications
Fgfr3 mutation disrupts chondrogenesis and bone ossification in zebrafish model mimicking CATSHL syndrome partially via enhanced Wnt/β-catenin signaling
Orthognathic surgery for patients with fibrous dysplasia involved with dentition | Maxillofacial Plastic and Reconstructive Surgery | Full Text
