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Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes. [electronic resource] by
- Pêgo, Sabina Pena B
- Coletta, Ricardo D
- Dumitriu, Simona
- Iancu, Daniela
- Albanyan, Saleh
- Kleta, Robert
- Auricchio, Maria Teresa
- Santos, Luis Antônio
- Rocha, Breno
- Martelli-Júnior, Hercílio
Producer: 20170918
In:
Oral surgery, oral medicine, oral pathology and oral radiology vol. 123
Availability: No items available.
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