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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 (> 9...

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Détails bibliographiques
Auteurs principaux: Varanasi, R, Bardeesy, N, Ghahremani, M, Petruzzi, M J, Nowak, N, Adam, M A, Grundy, P, Shows, T B, Pelletier, J
Format: Artigo
Langue:Inglês
Publié: 1994
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC43618/
https://ncbi.nlm.nih.gov/pubmed/8170946
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