Wilkes, M. J.
Loeys-Dietz syndrome caused by 1q41 deletion including TGFβ2 is associated with a neurodevelopmental phenotype
Tucker, M. E., Lyons, M. J., Demo, E., Wilkes, M. J., Fry, D., MacCarrick, G., Fleischer, J., Thomas, M. J., Groepper, D., and Steding, Catherine
Loeys-Dietz syndrome (LDS) is a connective tissue disorder that commonly results in a dilated aorta, aneurysms, joint laxity, craniosynostosis, and soft skin that bruises easily. Neurodevelopmental abnormalities are uncommon in...
Article
Work1
Article1
Steding, Catherine1
Demo, E.1
Fleischer, J.1
Fry, D.1
Groepper, D.1
1q41 deletion1
Loeys-Dietz syndrome1
TGFB21
developmental delay1
genetic testing1
English1
Wiley1
20221
Faculty Publications and Research - MUCOM1
Marian University1