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Dissecting the Wolf–Hirschhorn syndrome phenotype: WHSC1 is a neurodevelopmental gene contributing to growth delay, intellectual disability, and to the facial dysmorphism

Crossref DOI link: https://doi.org/10.1038/s10038-018-0476-1

Published Online: 2018-06-08

Published Print: 2018-08

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

Authors

Zollino, Marcella

Doronzio, Paolo Niccolo’
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Text and Data Mining valid from 2018-06-08
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Article History

Received: 15 May 2018

Revised: 15 May 2018

Accepted: 17 May 2018

First Online: 8 June 2018

Compliance with ethical standards

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: The authors declare that they have no conflict of interest.

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