Associated Papers
In utero tumor development and identification of CTNNB1 mutation in a newborn case of ossifying renal tumor of infancy.
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Supplement: supplement_1.xlsx › SNVs
Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome.
Ling C et al.
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Supplement: 12881_2018_725_MOESM2_ESM.xlsx › Sheet1
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