anchor instance (Q20437)

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    case highlights the need for a very detailed clinical assessment in patients with any suggestion of a
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    . Testing should be directed by phenotype but CCBE1 sequencing should be considered in even apparently
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    no value
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    17,452
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    26 March 2019
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    A novel CCBE1 mutation leading to a mild form of hennekam syndrome: case report and review of the literature (4630843)
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    no value
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