PTEN mutations and Proteus syndrome
Open Access
- 1 December 2001
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 358 (9298) , 2079-2080
- https://doi.org/10.1016/s0140-6736(01)07110-0
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden SyndromeHuman Molecular Genetics, 1999
- Mutation in GLI3 in postaxial polydactyly type ANature Genetics, 1997
- GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndromeNature Genetics, 1997