WNT5A mutations in patients with autosomal dominant Robinow syndrome (Q24317779)

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WNT5A mutations in patients with autosomal dominant Robinow syndrome
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    WNT5A mutations in patients with autosomal dominant Robinow syndrome (English)
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    Anthony D Person
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    Soraya Beiraghi
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    Christine M Sieben
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    Spencer Hermanson
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    Ann N Neumann
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    Mara E Robu
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    J Robert Schleiffarth
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    Charles J Billington
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    Jeannette M Hoogeboom
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    Juliana F Mazzeu
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    Anna Petryk
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    Stephen C Ekker
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    Jamie L Lohr
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    January 2010
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    239
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    1
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    327-37
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