A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
Background Orodental diseases include several clinically and genetically heterogeneous
disorders that can present in isolation or as part of a genetic syndrome. Due to the vast …
disorders that can present in isolation or as part of a genetic syndrome. Due to the vast …
Enamel–renal syndrome with congenital heart defects and asthma: a rare association in a Moroccan child
S Laouina, AB Zupan - Clinical dysmorphology, 2017 - journals.lww.com
Enamel–renal syndrome (ERS, OMIM 204690) is an autosomal recessive disorder
characterized by severe enamel hypoplasia on the primary and secondary dentition, pulp …
characterized by severe enamel hypoplasia on the primary and secondary dentition, pulp …
[HTML][HTML] A rare association-amelogenesis imperfecta, platispondyly and bicytopenia: a case report
S Laouina, S Chafai El Alaoui, R Amezian… - Journal of Medical Case …, 2015 - Springer
Introduction Amelogenesis imperfecta is an inherited disease characterized by generalized
structural abnormalities of the enamel on all teeth, including both primary and permanent …
structural abnormalities of the enamel on all teeth, including both primary and permanent …
[PDF][PDF] Etude clinique et moléculaire des amélogenèses imparfaites chez des familles marocaines
S Laouina - 2017 - toubkal.imist.ma
Les maladies rares sont définies par leur faible prévalence. Selon L'Union européenne
(UE), une maladie rare est une maladie qui touche moins d'une personne sur 2000. En …
(UE), une maladie rare est une maladie qui touche moins d'une personne sur 2000. En …
[CITATION][C] AMELOGENESE IMPARFAITE HEREDITAIRE: ETUDE CLINIQUE HISTOLOGIQUE ET/OU GENETIQUE
L SAMIR - 2016 - otrohati.imist.ma
AMELOGENESE IMPARFAITE HEREDITAIRE : ETUDE CLINIQUE HISTOLOGIQUE ET/OU
GENETIQUE Catalogue des thèses Marocaine en cour AMELOGENESE IMPARFAITE …
GENETIQUE Catalogue des thèses Marocaine en cour AMELOGENESE IMPARFAITE …