Associated Papers
Association of genetic variants, protein domains, and phenotypes in the ZMIZ1 syndromic neurodevelopmental disorder.
Cormier KE et al.
Frontiers in Neuroscience, 2025
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test.
Sheth F et al.
Bmc Neurology, 2023
37543562 (PubMed )
Supplement: 12883_2023_3341_MOESM1_ESM.xlsx › Primer_pairs
Select a paper to view details