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Results 1 - 8 of 8 for Noonan syndrome 6
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. RAF1 gene 
    ... to become cancerous. More than 25 mutations causing Noonan syndrome have been identified in the RAF1 gene. Noonan syndrome is characterized by mildly unusual facial characteristics, short ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  8. LRP2 gene 
    ... Kantarci S, Ragge NK, Thomas NS, Robinson DO, Noonan KM, Russell MK, Donnai D, Raymond FL, Walsh CA, Donahoe PK, Pober BR. Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous ...
    https://medlineplus.gov/genetics/gene/lrp2 - Genetics