Associated Papers
Prenatally detected encephalocele associated with a novel pathogenic TCTN3 variant: A case report and literature review.
Huljev Frković S et al.
American Journal of Medical Genetics. Part A, 2022
Meckel-Gruber Syndrome: Clinical and Molecular Genetic Profiles in Two Fetuses and Review of the Current Literature.
Turkyilmaz A et al.
Genetic Testing and Molecular Biomarkers, 2021
TCTN3 mutations cause Mohr-Majewski syndrome.
Thomas S et al.
American Journal of Human Genetics, 2012
Select a paper to view details