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http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_24/101093hmgddn294/authorship/7
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An Entity of Type :
vivo:Authorship
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scienceplus.abes.fr
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http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_24/101093hmgddn294/affiliation/af2
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Bale Sherri
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7
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Mutations in the human SIX3 gene in holoprosencephaly are loss of function
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