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Noonan syndrome: clinical features, diagnosis, and management guidelines.
Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Romano AA, et al. Among authors: noonan ja. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. Pediatrics. 2010. PMID: 20876176 Review.
Noonan syndrome--then and now.
Noonan J. Noonan J. Cardiol Young. 1999 Nov;9(6):545-6. doi: 10.1017/s1047951100005552. Cardiol Young. 1999. PMID: 10593261 No abstract available.
Adult height in Noonan syndrome.
Noonan JA, Raaijmakers R, Hall BD. Noonan JA, et al. Am J Med Genet A. 2003 Nov 15;123A(1):68-71. doi: 10.1002/ajmg.a.20502. Am J Med Genet A. 2003. PMID: 14556249
Noonan syndrome and related disorders: alterations in growth and puberty.
Noonan JA. Noonan JA. Rev Endocr Metab Disord. 2006 Dec;7(4):251-5. doi: 10.1007/s11154-006-9021-1. Rev Endocr Metab Disord. 2006. PMID: 17177115 Free PMC article. Review.
Noonan syndrome is a relatively common multiple malformation syndrome with characteristic facies, short stature and congenital heart disease, most commonly pulmonary stenosis (Noonan, Clin Pediatr, 33:548-555, 1994). Recently, a mutation in the PTPN11 gene (Tartagli
Noonan syndrome is a relatively common multiple malformation syndrome with characteristic facies, short stature and congenital heart
Noonan syndrome revisited.
Noonan JA. Noonan JA. J Pediatr. 1999 Dec;135(6):667-8. doi: 10.1016/s0022-3476(99)70082-x. J Pediatr. 1999. PMID: 10586166 No abstract available.
Cardio-facio-cutaneous syndrome: clinical features, diagnosis, and management guidelines.
Pierpont ME, Magoulas PL, Adi S, Kavamura MI, Neri G, Noonan J, Pierpont EI, Reinker K, Roberts AE, Shankar S, Sullivan J, Wolford M, Conger B, Santa Cruz M, Rauen KA. Pierpont ME, et al. Among authors: noonan j. Pediatrics. 2014 Oct;134(4):e1149-62. doi: 10.1542/peds.2013-3189. Epub 2014 Sep 1. Pediatrics. 2014. PMID: 25180280 Free PMC article. Review.
297 results