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                                       Details for article 14 of 240 found articles
 
 
  Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
 
 
Title: Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
Author: 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
Appeared in: Oral surgery, oral medicine, oral pathology and oral radiology
Paging: Volume 123 (2017) nr. 2 pages 23172 p.
Year: 2017
Contents:
Publisher: Elsevier Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 14 of 240 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands