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pdf:docinfo:title: De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
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dc:title: De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
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cp:subject: Genome Medicine 2013, 5:11. doi:10.1186/gm415
pdf:docinfo:subject: Genome Medicine 2013, 5:11. doi:10.1186/gm415
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description: Genome Medicine 2013, 5:11. doi:10.1186/gm415
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title: De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
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