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Germline mutation of the tumour suppressor PTEN in Proteus syndrome.
PMID: 12471211 [PubMed - indexed for MEDLINE]
PMCID: PMC1757209
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Cited by 4 PubMed Central articles
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Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.
Pezzolesi MG, Li Y, Zhou XP, Pilarski R, Shen L, Eng C.
Am J Hum Genet. 2006 Nov; 79(5):923-34. Epub 2006 Sep 29.
[Am J Hum Genet. 2006]
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ReviewBiomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis.
Timur AA, Driscoll DJ, Wang Q.
Cell Mol Life Sci. 2005 Jul; 62(13):1434-47.
[Cell Mol Life Sci. 2005]
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Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
Zhou XP, Marsh DJ, Morrison CD, Chaudhury AR, Maxwell M, Reifenberger G, Eng C.
Am J Hum Genet. 2003 Nov; 73(5):1191-8. Epub 2003 Oct 17.
[Am J Hum Genet. 2003]
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