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Article

Constellation of five facial features of tuberous sclerosis in a child with a TSC2 1808A>G mutation.

The oncologist - 1 Jan 2012

Hardy Rachel, Shepherd Charles W, Donnelly Deirdre E, McKee Shane A, Morrison Patrick J

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 22707510
DOI: 10.1634/theoncologist.2011-0407
PMCID: PMC3399647

Genes

TSC2

Provenance

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Related research

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Constellation of five facial features of tuberous sclerosis in a child with a TSC2 1808A>G mutation.PMID 22707510Read ↗

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A Patient with Coarse Facial Features and Molecular Odyssey: Lessons Learned and Best Practice.Semantic proximity Read ↗

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Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis.Semantic proximity Read ↗

Diagnosis of tuberous sclerosis complex in adulthood: a case reportSemantic proximity Read ↗

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