(Q34981090)
Statements
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SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype (English)
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G Spurlock
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E Bennett
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N Thomas
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H-Ping Jim
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L Side
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S Davies
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E Haan
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B Kerr
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S M Huson
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M Upadhyaya
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13 May 2009
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46
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7
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431-437
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Identifiers
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