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FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene
FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene
2020
Ayberk Turkyilmaz
Bilgen Bilge Geçkinli
Ceren Alavanda
Gülçin Zengin
Esra Arslan Ates
Ahmet Arman
Keywords:
Phenotype
Biology
Dysplasia
Genetics
Gene
LAMM syndrome
Correction
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