Research Explorer

Your browser does not support JavaScript or JavaScript is not enabled. Without JavaScript some functions of this webapplication may be disabled or cause error messages. To enable JavaScript, please consult the manual of your browser or contact your system administrator.

Project

Evaluation of the role of Myhre syndrome associated SMAD4 variants in neurodevelopment and fibrosis

Outputs and Outcomes

Publications

RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease

Maxim VerleeErika D'haenensLaurenz De CockLaura Muiño MosqueraKatya De GrooteKristof VandekerckhoveJoseph PanzerEllen RoetsBjörn MentenSofie SymoensPaul CouckeTim Van DammeSarah VergultBert Callewaert et al.

U Journal Article in EUROPEAN JOURNAL OF HUMAN GENETICS