Heterozygous FGFR1 mutation may be responsible for an incomplete form of osteoglophonic dysplasia, characterized only by radiolucent bone lesions and teeth retentions
| Autor: | Marzin, Pauline, Baujat, Geneviève, Gensburger, Déborah, Huber, Céline, Bole, Christine, Panuel, Michel, Finidori, Georges, De la Dure, Muriel, Cormier-Daire, Valérie |
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| Zdroj: | In European Journal of Medical Genetics February 2020 63(2) |
| Databáze: | ScienceDirect |
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