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Results 1 - 10 of 25 for Noonan syndrome 6
  1. Noonan syndrome 
    ... Testing Registry: Noonan syndrome 5 Genetic Testing Registry: Noonan syndrome 6 Genetic Testing Registry: Noonan syndrome 7 Genetic Testing ... NOONAN SYNDROME 8; NS8 NOONAN SYNDROME 7; NS7 NOONAN SYNDROME 6; NS6 NOONAN SYNDROME 9; NS9 NOONAN SYNDROME 10; ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. 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. ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  3. 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 ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  4. Baraitser-Winter syndrome 
    ... hypertelorism, and mental retardation: Baraitser-Winter syndrome or Noonan syndrome? J Med Genet. 1993 May;30(5):425-6. doi: 10.1136/jmg.30.5.425. Citation ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics
  5. PTPN11 gene 
    ... 2. Citation on PubMed Tartaglia M, Gelb BD. Noonan syndrome and related disorders: genetics and pathogenesis. Annu Rev Genomics Hum Genet. 2005;6:45-68. doi: 10.1146/annurev.genom.6. ...
    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 on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
  7. SOS1 gene 
    ... Kutsche K. SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. J Med Genet. 2007 Oct;44(10):651-6. doi: 10.1136/jmg.2007.051276. Epub 2007 ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  8. Cardiofaciocutaneous syndrome 
    ... Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833-42. doi: 10.1136/jmg.2006.042796. Epub 2006 Jul 6. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  9. MAP2K1 gene 
    ... cell histiocytosis. Genes Chromosomes Cancer. 2015 Jun;54(6):361-8. doi: ... in a patient with Noonan syndrome with multiple lentigines. Am J Med Genet A. ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  10. RIT1 gene 
    ... the RIT1 gene have been found to cause Noonan syndrome. This condition is characterized by mildly unusual facial ... and many other signs and symptoms. People with Noonan syndrome caused by RIT1 gene mutations often have swelling ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
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