(Q50304924)
Statements
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Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screening. (English)
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Maximilian Handt
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Andrea Epplen
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Sabine Hoffjan
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Kemal Mese
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Jörg T Epplen
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Gabriele Dekomien
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27 August 2014
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28
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5-6
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279-283
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Identifiers
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