Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects (Q28306581)

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Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects
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    Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects (English)
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    Kathleen A Williamson
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    Joe Rainger
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    James A B Floyd
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    Morad Ansari
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    Alison Meynert
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    Kishan V Aldridge
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    Jacqueline K Rainger
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    Anthony T Moore
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    Angus Clarke
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    6 February 2014
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    94
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    2
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    295-302
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