Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia (Q24307279)

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Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia
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    Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia (English)
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    Eissa Ali Faqeih
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    Zvi Borochowitz
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    Denise P Cavalcanti
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    Amandine Frigo
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    Patrick Nitschke
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    Heloísa G Santos
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    Stavit A Shalev
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    10 January 2013
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    92
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    1
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    144-9
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