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Results 1 - 10 of 31 for Noonan syndrome 10
  1. Noonan syndrome 
    ... Testing Registry: Noonan syndrome 1 Genetic Testing Registry: Noonan syndrome 10 Genetic Testing Registry: Noonan syndrome 2 Genetic Testing ... NOONAN SYNDROME 6; NS6 NOONAN SYNDROME 9; NS9 NOONAN SYNDROME 10; NS10 PubMed Chen PC, Yin J, Yu HW, ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. SOS1 gene 
    ... Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Nat Genet. 2007 Jan;39(1):70-4. doi: 10.1038/ng1926. Epub 2006 Dec 3. Citation on ... function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat ... 2007 Jan;39(1):75-9. doi: 10.1038/ng1939. Epub 2006 Dec 13. Erratum In: ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  3. KRAS gene 
    ... Shannon K, Kratz CP. Germline KRAS mutations cause Noonan syndrome. Nat Genet. 2006 Mar;38(3):331-6. doi: 10.1038/ng1748. Epub 2006 Feb 12. Erratum In: ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  4. RAF1 gene 
    ... Germline gain-of-function mutations in RAF1 cause Noonan syndrome. Nat Genet. 2007 Aug;39(8):1013-7. doi: 10.1038/ng2078. Epub 2007 Jul 1. Citation on ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  5. PTPN11 gene 
    ... mutations in PTPN11 gene in two girls with Noonan syndrome phenotype. Int J Cardiol. 2015;186:13-5. doi: 10.1016/j.ijcard.2015.03.260. Epub 2015 ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical ... 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  6. NRAS gene 
    ... M. A restricted spectrum of NRAS mutations causes Noonan syndrome. Nat Genet. 2010 Jan;42(1):27-9. doi: 10.1038/ng.497. Epub 2009 Dec 6. Citation ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical ... 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
  7. Neurofibromatosis type 1 
    ... mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome. Am J Hum Genet. 2005 Dec;77(6):1092-101. doi: 10.1086/498454. Epub 2005 Oct 26. Citation on ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  8. RIT1 gene 
    ... Zenker M. Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation. Genet Med. 2016 Dec;18(12):1226-1234. doi: 10.1038/gim.2016.32. Epub 2016 Apr 21. ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
  9. Noonan syndrome with multiple lentigines 
    ... 2014 Jul 1;53(25):4136-51. doi: 10.1021/bi5002695. Epub 2014 Jun 17. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  10. BRAF gene 
    ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
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