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

Marcella Zollino; Paolo Niccolo Doronzio

doi:10.1038/s10038-018-0476-1

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

Marcella Zollino, Paolo Niccolo Doronzio

IRCCS Fondazione Policlinico Universitario A. Gemelli

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English
Pages (from-to)	859-861
Number of pages	3
Journal	Journal of Human Genetics
Volume	63
Issue number	8
DOIs	https://doi.org/10.1038/s10038-018-0476-1
Publication status	Published - Jul 1 2018

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1038/s10038-018-0476-1

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

author = "Marcella Zollino and Doronzio, {Paolo Niccolo}",

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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

ASJC Scopus subject areas

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