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bibliographicCitation Ekvall S, Hagenäs L, Allanson J, Annerén G, Bondeson M. Co‐occurring SHOC2 and PTPN11 mutations in a patient with severe/complex Noonan syndrome‐like phenotype. American J of Med Genetics Pt A. 2011 May 05;155(6):1217–24. doi: 10.1002/ajmg.a.33987.
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title Co‐occurring SHOC2 and PTPN11 mutations in a patient with severe/complex Noonan syndrome‐like phenotype
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