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[Noonan Syndrome (NS) is an autosomal dominant condition characterized by short stature, facial dysmorphisms, and congenital heart defects, and is caused by mutations in either PTPN11, KRAS, NRAS, SHOC2, RAF1, or SOS1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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