FGF Signaling in Cartilage Development and Disease
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Publisher
Elsevier
Reference235 articles.
1. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23;ADHR Consortium;Nature Genetics,2000
2. Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis;Agochukwu;Pediatric Neurology,2012
3. Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders;Bai;Endocrinology,2004
4. Mild isolated craniosynostosis due to a novel FGFR3 mutation, p.Ala334Thr;Barroso;American Journal of Medical Genetics. Part A,2011
5. The PTH-Vitamin D-FGF23 axis;Blau;Reviews in Endocrine & Metabolic Disorders,2015
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