(Q43076033)
Statements
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Incidence and molecular mechanism of aberrant splicing owing to a G-->C splice acceptor site mutation causing Smith-Lemli-Opitz syndrome (English)
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Waterham HR
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Oostheim W
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Romeijn GJ
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Wanders RJ
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Hennekam RC
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1 May 2000
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37
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387-389
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Identifiers
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