Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signalingAlexander M. Holtz, Benjamin A. Raby, Richard Person et al.|Genetics in Medicine|2022Cited by 23
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative ReviewElizabeth VanSickle, Caleb Bupp, Sara M. Sarasua et al.|American Journal of Medical Genetics Part A|2025Cited by 1
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative ReviewElizabeth VanSickle, Caleb P. Bupp, Sara M. Sarasua et al.|Unknown|2026Cited by 0
Cover Image, Volume 200A, Number 5, May 2026Elizabeth VanSickle, Caleb Bupp, Sara M. Sarasua et al.|American Journal of Medical Genetics Part A|2026Cited by 0