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Article

Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations.

Clinical dysmorphology - 1 Jul 2010

Slezak Ryszard, Luczak Klaudiusz, Kalscheuer Vera, Neumann Thomas E, Sasiadek Maria M

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Source

Identifiers

PMID: 20305546
DOI: 10.1097/MCD.0b013e3283375886

Genes

SOS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations.PMID 20305546Read ↗

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<i>SOS1</i> is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndromeSemantic proximity Read ↗

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Multiple versus solitary giant cell lesions of the jaw: Similar or distinct entities?Semantic proximity Read ↗

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Variable phenotypic expression in a large Noonan syndrome family segregating a novel SOS1 mutation.Semantic proximity Read ↗

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