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Article

Prenatal diagnosis of hypoplastic left heart syndrome associated with Noonan Syndrome and de novo RAF1 mutation.

Prenatal diagnosis - 1 Oct 2012

Schulz Solveig, Fröber Rosemarie, Kraus Cornelia, Schneider Uwe

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Proto-Oncogene Proteins c-raf

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Source

Identifiers

PMID: 22821648
DOI: 10.1002/pd.3938

Genes

RAF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Research trail→

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Prenatal diagnosis of hypoplastic left heart syndrome associated with Noonan Syndrome and de novo RAF1 mutation.PMID 22821648Read ↗

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Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant.Semantic proximity Read ↗

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Noonan syndrome: improving recognition and diagnosis.Semantic proximity Read ↗

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