Fine structure analysis of the WT1 gene in sporadic Wilms tumors.
Molecular genetic studies indicate that the etiology of Wilms tumor (WT) is complex, involving at least three loci. Germ-line mutations in the tumor suppressor gene, WT1, have been documented in children with WTs and urogenital developmental anomalies. Sporadic tumors constitute the majority (> 90%)...
Salvato in:
| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
1994
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC43618/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8170946/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.9.3554 |
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