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                                       Details for article 81 of 162 found articles
 
 
  Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families
 
 
Title: Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families
Author: Dourado, Mauricio Rocha
dos Santos, Cássio Roberto Rocha
Dumitriu, Simona
Iancu, Daniela
Albanyan, Saleh
Kleta, Robert
Coletta, Ricardo D.
Marques Mesquita, Ana Terezinha
Appeared in: European journal of medical genetics
Paging: Volume 62 (2019) nr. 11 pages p.
Year: 2019
Contents:
Publisher: Elsevier Masson SAS
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 81 of 162 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands