Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions (Q28260716)

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Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions
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    Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions (English)
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    Pia Vuorela
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    Sirpa Ala-Mello
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    Carola Saloranta
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    Maila Penttinen
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    Minna Pöyhönen
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    Kirsi Huoponen
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    Wiktor Borozdin
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    Birke Bausch
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    Elke M Botzenhart
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    Christian Wilhelm
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    Jürgen Kohlhase
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    October 2007
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    9
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    10
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    690-4
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