Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
about
Amelogenesis imperfecta and anterior open bite: Etiological, classification, clinical and management interrelationships.Fam83h null mice support a neomorphic mechanism for human ADHCAIEffects of Fam83h overexpression on enamel and dentine formation.Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta.Amelogenin gene influence on enamel defects of cleft lip and palate patients.
P2860
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
description
2011 nî lūn-bûn
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name
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@en
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@nl
type
label
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@en
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@nl
prefLabel
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@en
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@nl
P2093
P2860
P1476
Limited phenotypic variation o ...... ovel FAM83H nonsense mutation.
@en
P2093
Anders D Børglum
Dorte Haubek
Hans Gjørup
Inger Juncker
Lillian G Jensen
Sven Poulsen
P2860
P304
P356
10.1111/J.1365-263X.2011.01142.X
P407
P577
2011-06-27T00:00:00Z