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UnknownWhole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta.
Not available
S-EPMC3865405 | biostudies-literature
UnknownAmelogenesis Imperfecta; Genes, Proteins, and Pathways.
Not available
S-EPMC5483479 | biostudies-literature
UnknownAssociation of a null allele of SPRN with variant Creutzfeldt-Jakob disease.
Not available
S-EPMC2590874 | biostudies-literature
UnknownSelf-rated health scores predict mortality among people with type 2 diabetes differently across three different country groupings: findings from the ADVANCE and ADVANCE-ON trials.
Not available
S-EPMC7496988 | biostudies-literature
UnknownA missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta.
Not available
S-EPMC3959822 | biostudies-literature
UnknownA Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities.
Not available
S-EPMC5447068 | biostudies-literature
UnknownOptimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in.
Not available
S-EPMC6775134 | biostudies-literature
UnknownDeletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.
Not available
S-EPMC5179951 | biostudies-literature
UnknownTopological data analysis quantifies biological nano-structure from single molecule localization microscopy.
Not available
S-EPMC7162425 | biostudies-literature
UnknownDefects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.
Not available
S-EPMC5511509 | biostudies-literature
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