Associated Papers
Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations.
Bugueno IM et al.
Genes & Diseases, 2024
38721411 (PubMed )
Supplement: mmc2.pdf
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants.
Tuncay IO et al.
Npj Genomic Medicine, 2022
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 452.202
Select a paper to view details