Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
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, HercílioVolume:
123
Language:
english
Journal:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
DOI:
10.1016/j.oooo.2016.09.226
Date:
February, 2017
File:
PDF, 7.08 MB
english, 2017