BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Titel:
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Auteur:
Breckpot, Jeroen Tranchevent, Léon-Charles Thienpont, Bernard Bauters, Marijke Troost, Els Gewillig, Marc Vermeesch, Joris R. Moreau, Yves Devriendt, Koenraad Van Esch, Hilde