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Article

A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome

6 Oct 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15470362
DOI: 10.1038/sj.ejhg.5201290

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Related research

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A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndromePMID 15470362Read ↗

Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 GeneSemantic proximity Read ↗

Coexisting PTPN11 and TNNT2 mutations in noonan syndrome with multiple lentigines.Semantic proximity Read ↗

Noonan syndrome and related disorders: genetics and pathogenesis.Semantic proximity Read ↗

Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome.Semantic proximity Read ↗

[Noonan syndrome and Leopard syndrome linked to mutation of the gene PTPN11].Semantic proximity Read ↗

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.Semantic proximity Read ↗

PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype.Semantic proximity Read ↗

PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.Semantic proximity Read ↗

LEOPARD Syndrome: Clinical Features and Gene MutationsSemantic proximity Read ↗

[Noonan's syndrome caused by a mutation in the PTPN11 gene].Semantic proximity Read ↗

PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.Semantic proximity Read ↗

A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions.Semantic proximity Read ↗

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