Associated Papers
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients.
Watts LM et al.
European Journal of Human Genetics : Ejhg, 2024
38760421 (PubMed )
Supplement: 41431_2024_1624_MOESM3_ESM.xlsx › Sheet1
Genetic basis of human left-right asymmetry disorders.
Deng H et al.
Expert Reviews in Molecular Medicine, 2015
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.
Twigg SR et al.
American Journal of Human Genetics, 2012
Select a paper to view details