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Statements

Subject Item

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A Noonan syndrome that has_material_basis_in aused by heterozygous mutation in the RIT1 gene on chromosome 1q22.

obo:hasDbXref

url:https://www.ncbi.nlm.nih.gov/pubmed/24939608 url:https://www.ncbi.nlm.nih.gov/pubmed/25124994