The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2

por Peeters, Silke, De Kinderen, Pauline, Meester, Josephina A. N., Verstraeten, Aline, Loeys, Bart L.
Publicado 2022

IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type)

por De Kinderen, Pauline, Peeters, Silke, Rabaut, Laura, Mortier, Geert, Ponsaerts, Peter, Loeys, Bart, Verstraeten, Aline, Meester, Josephina A.N.
Publicado 2023

IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)

por De Kinderen, Pauline, Rabaut, Laura, Perik, Melanie H.A.M., Peeters, Silke, Ponsaerts, Peter, Loeys, Bart, Mortier, Geert, Meester, Josephina A.N., Verstraeten, Aline
Publicado 2023