(Q43073334)
Statements
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Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease (English)
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Munnich A
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Lathrop M
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Pelet A
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de Pontual L
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Clément-Ziza M
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Salomon R
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Mugnier C
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Matsuda F
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Feingold J
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Abel L
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1 March 2005
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42
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e18
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Identifiers
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