Further Analysis of the Crouzon Mouse: Effects of the FGFR2 super(C342Y) Mutation Are Cranial Bone-D...
Further Analysis of the Crouzon Mouse: Effects of the FGFR2 super(C342Y) Mutation Are Cranial Bone-Dependent
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English
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Crouzon syndrome is a debilitating congenital disorder involving abnormal craniofacial skeletal development caused by mutations in fibroblast growth factor receptor-2 (FGFR2). Phenotypic expression in humans exhibits an autosomal dominant pattern that commonly involves premature fusion of the coronal suture (craniosynostosis) and severe midface hyp...
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Further Analysis of the Crouzon Mouse: Effects of the FGFR2 super(C342Y) Mutation Are Cranial Bone-Dependent
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TN_cdi_proquest_miscellaneous_1352288618
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1352288618
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ISSN
0171-967X
E-ISSN
1432-0827
DOI
10.1007/s00223-013-9701-2
