(Q34158548)
Statements
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Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A. (English)
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Eliot L Berson
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Thaddeus P Dryja
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1 November 2002
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120
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11
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1566-1571
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Identifiers
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