Associated Papers
Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Nitayavardhana I et al.
Molecular Genetics and Genomics : Mgg, 2020
Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation.
Kantaputra PN et al.
American Journal of Medical Genetics. Part A, 2014
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