Associated Papers
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families.
Greenbaum L et al.
Frontiers in Genetics, 2019
Compound Heterozygosity for Novel Truncating Variants in the LMOD3 Gene as the Cause of Polyhydramnios in Two Successive Fetuses.
Wang Y et al.
Frontiers in Genetics, 2019
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
Yuen M et al.
The Journal of Clinical Investigation, 2015
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
Yuen M et al.
The Journal of Clinical Investigation, 2014
Select a paper to view details