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Results 1 - 10 of 35 for Noonan syndrome 3
  1. Noonan syndrome 
    ... Testing Registry: Noonan syndrome 2 Genetic Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 Genetic Testing ... NOONAN SYNDROME 2; NS2 NOONAN SYNDROME 4; NS4 NOONAN SYNDROME 3; NS3 NOONAN SYNDROME 5; NS5 NOONAN SYNDROME 8; ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. Cardiofaciocutaneous syndrome 
    ... of two other genetic conditions, Costello syndrome and Noonan syndrome. The three conditions are distinguished by their genetic cause and ... Genet A. 2006 Aug 1;140(15):1681-3. doi: 10.1002/ajmg.a.31315. No abstract ... T, Neri G. The cardiofaciocutaneous syndrome. J Med Genet. 2006 Nov;43(11):833- ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  3. Noonan syndrome with multiple lentigines 
    ... Registry: LEOPARD syndrome 2 Genetic Testing Registry: LEOPARD syndrome 3 Genetic Testing Registry: Noonan syndrome with multiple lentigines LEOPARD syndrome National Organization ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  4. 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 ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  5. 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 PubMed Romano AA, Allanson JE, Dahlgren ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  6. Costello syndrome 
    ... other genetic conditions, cardiofaciocutaneous syndrome (CFC syndrome) and Noonan syndrome. In affected infants, it can be difficult to tell the three conditions apart based on their physical features. However, ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  7. RAF1 gene 
    ... Y. Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation. Hum Mutat. 2010 Mar;31(3):284-94. doi: 10.1002/humu.21187. Citation ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  8. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    Cardiomyopathy/Children ... Cardiomyopathy ... Children's Cardiomyopathy Foundation
    https://www.childrenscardiomyopathy.org/pages/about-disease/causes - External Health Links
  9. RIT1 gene 
    ... the Ras family of oncogenes, which also includes three other genes: KRAS, HRAS, and NRAS. These ... found to cause Noonan syndrome. This condition is characterized by mildly unusual facial ...
    https://medlineplus.gov/genetics/gene/rit1 - Genetics
  10. MAP2K1 gene 
    ... novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple ... syndrome. Science. 2006 Mar 3;311(5765):1287-90. doi: 10.1126/science. ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
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