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Results 1 - 6 of 6 for Noonan syndrome 13
  1. 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 Mar 19. No abstract available. Citation on PubMed ... Collaborative Noonan Study Group. PTPN11 mutations in patients with LEOPARD ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  2. SOS1 gene 
    ... function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet. 2007 Jan;39(1):75-9. doi: 10.1038/ng1939. Epub 2006 Dec 13. Citation on PubMed Zenker M, Horn D, Wieczorek ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  3. KRAS gene 
    ... This Health Condition MedlinePlus Genetics provides information about Noonan syndrome More About This Health Condition MedlinePlus Genetics provides ... syndrome (described above) and two related disorders called Noonan syndrome and Costello syndrome. This condition has been described ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  4. MAP2K1 gene 
    ... the MAP2K1 gene has been found to cause Noonan syndrome with multiple lentigines (formerly called LEOPARD syndrome). This ... and tissues, resulting in the characteristic features of Noonan syndrome with multiple lentigines.It is unclear why the ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  5. MAP2K2 gene 
    ... Verloes A, Cave H. Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling ...
    https://medlineplus.gov/genetics/gene/map2k2 - Genetics
  6. LZTR1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Noonan syndrome More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/lztr1 - Genetics