Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome
Josephina Meester(University of Antwerp), Bart Loeys(Radboud University Nijmegen)
Cited by 4
Related Papers
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
|Nature Genetics|2005|1.8k
Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections
|Journal of the American College of Cardiology|2015|292
Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
|European Journal of Human Genetics|2010|151