Co-occurring SHOC2 and PTPN11 mutations in a patient with severe/complex Noonan syndrome-like phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33987/fullpdf
Reference26 articles.
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2. Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia;Bentires-Alj;Cancer Res,2004
3. Neurofibromatosis-Noonan syndrome:Molecular evidence of the concurrence of both disorders in a patient;Bertola;Am J Med Genet Part A,2005
4. PTPN11 and KRAS gene analysis in patients with Noonan and Noonan-like syndromes;Brasil;Genet Test Mol Biomarkers,2010
5. Paravertebral mass in a patient with hemolytic anemia:Computed tomographic findings;Carvalho;Case Rep Med,2010
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