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KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome

Crossref DOI link: https://doi.org/10.1186/s12881-015-0211-0

Published Online: 2015-08-22

Published Print: 2015-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Moreno-Igoa, María

Hernández-Charro, Blanca

Bengoa-Alonso, Amaya

Pérez-Juana-del-Casal, Aranzazu

Romero-Ibarra, Carlos

Nieva-Echebarria, Beatriz

Ramos-Arroyo, María Antonia
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License valid from 2015-08-22