Associated Papers
A Novel Missense Mutation in the FGF3 Gene of a Chinese Patient with LAMM Syndrome.
Zhang K et al.
Biochemical Genetics, 2025
Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review.
Jamshidi F et al.
Molecular Genetics & Genomic Medicine, 2023
Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss.
Lallar M et al.
Journal of Pediatric Genetics, 2021
Single gene variants causing deafness in Asian Indians.
Panigrahi I et al.
Journal of Genetics, 2021
Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases.
Al Yassin A et al.
Genes, 2019
Delayed presentation of rickets in a child with labyrinthine aplasia, microtia and microdontia (LAMM) syndrome.
Singh A et al.
Indian Pediatrics, 2014
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