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C Mehawej

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European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|August 20, 2022
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese populationR Elzein, F Abdel-Sater, C Mehawej, et al.
Molecular Syndromology|March 5, 2011
Molecular Study of Three Lebanese and Syrian Patients with Waardenburg Syndrome and Report of Novel Mutations in the EDNRB and MITF GenesN M Haddad, D Ente, E Chouery, et al.
Clinical Genetics|November 3, 2017
Homozygous mutation in ELMO2 may cause Ramon syndromeC Mehawej, A Hoischen, R A Farah, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|August 20, 2022
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese populationR Elzein, F Abdel-Sater, C Mehawej, et al.
Molecular Syndromology|March 5, 2011
Molecular Study of Three Lebanese and Syrian Patients with Waardenburg Syndrome and Report of Novel Mutations in the EDNRB and MITF GenesN M Haddad, D Ente, E Chouery, et al.
Clinical Genetics|November 3, 2017
Homozygous mutation in ELMO2 may cause Ramon syndromeC Mehawej, A Hoischen, R A Farah, et al.
Pageof 1