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Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity
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| Main Authors: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Group
2000
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734594/ https://ncbi.nlm.nih.gov/pubmed/10905890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.5.377 |
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