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Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

✍ Scribed by Zollino, Marcella; Orteschi, Daniela; Murdolo, Marina; Lattante, Serena; Battaglia, Domenica; Stefanini, Chiara; Mercuri, Eugenio; Chiurazzi, Pietro; Neri, Giovanni; Marangi, Giuseppe

Book ID: 120451638
Publisher: Nature Publishing Group
Year: 2012
Tongue: English
Weight: 298 KB
Volume: 44
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.2257

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