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Results 1 - 5 of 5 for Noonan syndrome 11
  1. PTPN11 gene 
    ... time. BPTP3 protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1) protein-tyrosine phosphatase 2C PTN11_HUMAN PTP- ... Baumann C, Verloes A, Cave H; French Collaborative Noonan Study Group. PTPN11 ... J Med Genet. 2004 Nov;41(11):e117. doi: 10.1136/jmg.2004.021451. No ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  2. MAP2K1 gene 
    ... novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines. Am J Med Genet A. 2015 Feb;167A(2):407-11. doi: 10.1002/ajmg.a.36842. Epub 2014 ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  3. KRAS gene 
    ... Martinez AF, Kruszka P, Muenke M. Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature. Am J Med Genet A. 2015 Nov;167A(11):2657-63. doi: 10.1002/ajmg.a.37259. ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  4. BRAF gene 
    ... Rev Oncol Hematol. 2015 Jul;95(1):1-11. doi: 10.1016/j.critrevonc.2015.02.004. Epub ... Tartaglia M. Noonan Syndrome with Multiple Lentigines. 2007 Nov 30 [updated 2022 ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
  5. DYNC2H1 gene 
    ... also known as Verma-Naumoff syndrome or Saldino-Noonan syndrome. These disorders have signs and symptoms similar to ... cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III. Am J Hum Genet. 2009 May;84(5):706-11. doi: 10.1016/j.ajhg.2009.04.016. ...
    https://medlineplus.gov/genetics/gene/dync2h1 - Genetics