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The Wilms’ tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes

✍ Scribed by Tamaki, H; Ogawa, H; Ohyashiki, K; Ohyashiki, JH; Iwama, H; Inoue, K; Soma, T; Oka, Y; Tatekawa, T; Oji, Y

Book ID
110054138
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
107 KB
Volume
13
Category
Article
ISSN
0887-6924

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The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
✍ Angela S. Barbosa; Charalambos G. Hadjiathanasiou; Charalambos Theodoridis; Asté 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 464 KB 👁 2 views

Communicated by Michel Goossens ## Denys -Drash and Frasier syndromes are rare human disorders that associate nephropathy with gonadal and genital abnormalities. In DDS there is a predisposition to Wilms tumor. Heterozygous point mutations in the Wilms tumor, type1 gene (WT1), particularly those