Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/1472-6831-15-14
Published Online: 2015-01-30
Published Print: 2015-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Cherkaoui Jaouad, Imane
El Alloussi, Mustapha
Chafai El alaoui, Siham
Laarabi, Fatima Zahra
Lyahyai, Jaber
Sefiani, Abdelaziz
License valid from 2015-01-30
Article History
Received: 21 September 2014
Accepted: 19 January 2015
First Online: 30 January 2015