Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis (Q29144905)
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English | Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis |
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Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis (English)
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Deborah A Nickerson
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Lisa Maves
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Brig Mecham
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University of Washington Center for Mendelian Genomics
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Joshua D Smith
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Anne V Hing
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Christine M Clarke
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Nathan M Johnson
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Francisco A Perez
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Sarah S Park
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Jeremy A Horst
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Michael L Cunningham
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1 August 2014
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95
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235-240
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