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Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

✍ Scribed by Rahman, Nazneen; Arbour, Laura; Tonin, Patricia; Renshaw, Jane; Pelletier, Jerry; Baruchel, Sylvain; Pritchard-Jones, Kathryn; Stratton, Michael R.; Narod, Steven A.


Book ID
109916726
Publisher
Nature Publishing Group
Year
1996
Tongue
English
Weight
301 KB
Volume
13
Category
Article
ISSN
1061-4036

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✍ Froelich, Susanne; Basun, Hans; Forsell, Charlotte; Lilius, Lena; Axelman, Karin 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 58 KB 👁 2 views

Familial frontotemporal dementia (FTD) is a complex disorder with lack of distinctive histopathological markers found in other types of dementia. Most of the linkage reports from FTD families map the disease loci to chromosome 17q21-22. However, FTD is genetically heterogeneous, as linkage also has