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Filatova, Alina and Rey, Linda K. and Lechler, Marion B. and Schaper, Jörg and Hempel, Maja and Posmyk, Renata and Szczaluba, Krzysztof and Santen, Gijs W. E. and Wieczorek, Dagmar and 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), p. 2966, ISSN 2041-1723,
DOI: 10.1038/s41467-019-10849-y,
[Article]

This list was generated on Tue Aug 4 01:36:43 2020 CEST.