Cowden's disease with a defined genetic alteration--chromosomal duplication at 15q11-q13
Cowden's disease with a defined genetic alteration--chromosomal duplication at 15q11-q13
About this item
Full title
Author / Creator
Suzuki, T , Ichinose, M , Matsubara, Y , Yahagi, N , Kurokawa, K , Fukamachi, H and Miki, K
Publisher
Japan: Springer Nature B.V
Journal title
Language
English
Formats
Publication information
Publisher
Japan: Springer Nature B.V
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Scope and Contents
Contents
Cowden's disease, multiple hamartoma syndrome, is a dominantly inherited disorder characterized by multiple hamartomas of ectodermal, endodermal, and mesodermal origin and also by a high incidence of malignant tumors. Despite many efforts to identify the genetic alterations responsible for the syndrome, the molecular mechanism remains unclear. We r...
Alternative Titles
Full title
Cowden's disease with a defined genetic alteration--chromosomal duplication at 15q11-q13
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_79370499
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_79370499
Other Identifiers
ISSN
0944-1174
E-ISSN
1435-5922
DOI
10.1007/BF02934124
