Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function (Q36435480)

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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
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    Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function (English)
    J Clayton-Smith
    R C M Hennekam
    M-J H van den Boogaard
    A van Haeringen
    C T R M Schrander-Stumpel
    D M McDonald-McGinn

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