Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
Publication year
1999Source
European Journal of Human Genetics, 7, 3, (1999), pp. 267-273ISSN
Publication type
Article / Letter to editor

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Organization
Cell Biology (UMC)
Otorhinolaryngology
Physiology
Human Genetics
Neurology
Journal title
European Journal of Human Genetics
Volume
vol. 7
Issue
iss. 3
Page start
p. 267
Page end
p. 273
Subject
Clinical and genetic studies in Cowden disease.; Positional cloning of the gene for Cowden disease and investigating the importance of mutations in this gene for the development of various tumors; Klinisch en genetisch onderzoek bij de ziekte van Cowden.; Positionele clonering van het gen voor de ziekte van Cowden en onderzoek naar de rol van mutaties in dit gen bij een aantal typen tumorenThis item appears in the following Collection(s)
- Academic publications [227088]
- Faculty of Medical Sciences [86606]
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