Fgfr3 mutation disrupts chondrogenesis and bone ossification in zebrafish model mimicking CATSHL syndrome partially via enhanced Wnt/β-catenin signaling
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![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
JCM | Free Full-Text | Stem Cells Regenerating the Craniofacial Skeleton: Current State-Of-The-Art and Future Directions
Frontiers | Bone Phenotyping Approaches in Human, Mice and Zebrafish – Expert Overview of the EU Cost Action GEMSTONE (“GEnomics of MusculoSkeletal traits TranslatiOnal NEtwork”)
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Osteochondrodysplasia disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
PDF) Bone markers in craniofacial bone deformations and dysplasias
Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling | Nature Communications
Markers for specific skeletal stem cell populations. a In long bones,... | Download Scientific Diagram
Gαs signaling controls intramembranous ossification during cranial bone development by regulating both Hedgehog and Wnt/β-catenin signaling | Bone Research
Fibrous dysplasia of bone: craniofacial and dental implications - Burke - 2017 - Oral Diseases - Wiley Online Library
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Craniofacial Fibrous Dysplasia | Children's Hospital of Philadelphia
Frontiers | A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders
High bone resorption | International Osteoporosis Foundation
Craniofacial Manifestations of Systemic Disorders: CT and MR Imaging Findings and Imaging Approach | RadioGraphics
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
Genetics of craniofacial development and malformation | Nature Reviews Genetics
