Associated Papers
A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3.
Flex E et al.
Genes, 2021
34573388 (PubMed )
Supplement: genes-12-01406-s001.zip › genes-1354874-supplementary.pdf
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.
Matsunami N et al.
Molecular Autism, 2014
Select a paper to view details