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Gene Pair Information
Gene Pair: H19, CDKN1C
Related Sentences
# |
PMID |
Sentence |
1 |
11813134
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The most common constitutional abnormalities in BWS are epigenetic, involving abnormal methylation of either H19 or LIT1, which encode untranslated RNAs on 11p15.
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2 |
11813134
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These results define an epigenotype-phenotype relationship in BWS, in which aberrant methylation of H19 and LIT1 and UPD are strongly associated with cancer risk and specific birth defects.
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