Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

por Alina Filatova, Linda K. Rey, Marion B. Lechler, Jörg Schaper, Maja Hempel, Renata Posmyk, Krzysztof Szczaluba, Gijs W. E. Santen, Dagmar Wieczorek, Ulrike A. Nuber
Publicado 2019