Results 121 to 130 of about 6,417 (245)
Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta [PDF]
Background: Amelogenesis imperfecta (AI) is an inherited disorder characterized by abnormal formation of tooth enamel. Although several genes responsible for AI have been reported, not all causative genes for human AI have been identified to date.
Hagita, Hiroko+4 more
core
Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta. [PDF]
Zhang Z+10 more
europepmc +1 more source
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta [PDF]
Maria Cristina Leme Godoy dos Santos+5 more
openalex +1 more source
FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta [PDF]
Jung‐Wook Kim+9 more
openalex +1 more source
Amelogenesis Imperfecta: A Review [PDF]
Pulivarthi Sushma+3 more
openaire +1 more source
Effect of acid etching time on bond strength of an etch‐and‐rinse adhesive to primary tooth dentine affected by amelogenesis imperfecta [PDF]
Noriko Hiraishi+2 more
openalex +1 more source
Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta [PDF]
David Parry+19 more
openalex +1 more source
sumen Objetivo. Describir el manejo clínico para la restauración estética y funcional de un caso con amelogénesis imperfecta. Caso clínico. Paciente femenina de 15 años que presentaba alteración en la apariencia estética de sus dientes y episodios ...
Weider de Oliveira+5 more
doaj