Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis
<p>Abstract</p> <p>Background</p> <p>Hirschsprung's disease (HSCR) is a classic oligogenic disorder. Except inactivating mutations of RET, some single nucleotide polymorphisms (SNPs) are identified to be associated with the risk of HSCR. This study was conducted to...
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BMC,
2011-02-01T00:00:00Z.
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A1234.567 |
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Kopie 1 | Beschikbaar |