Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. (Q34325459)
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English | Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. |
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Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. (English)
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Shanske A
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Ferreira JC
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Leonard JC
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Fuller P
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Marion RW
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1 August 2001
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102
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3
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231-236
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