Filatova, Alina ; Rey, Linda K. ; Lechler, Marion B. ; Schaper, Jörg ; Hempel, Maja ; Posmyk, Renata ; Szczaluba, Krzysztof ; Santen, Gijs W. E. ; Wieczorek, Dagmar ; Nuber, Ulrike A. (2019)
Mutations in SMARCB1 and in other Coffin-Siris syndrome genes lead to various brain midline defects.
In: Nature communications, 10 (1)
doi: 10.1038/s41467-019-10849-y
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