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Results 1 - 10 of 15 for Noonan syndrome 11
  1. PTPN11 gene 
    ... time. BPTP3 protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1) protein-tyrosine phosphatase 2C PTN11_HUMAN PTP- ... Baumann C, Verloes A, Cave H; French Collaborative Noonan Study Group. PTPN11 ... J Med Genet. 2004 Nov;41(11):e117. doi: 10.1136/jmg.2004.021451. No ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  2. Noonan syndrome 
    ... Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome. Hum Mutat. 2015 Nov;36(11):1080-7. doi: 10.1002/humu.22834. Epub ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  3. MAP2K1 gene 
    ... novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines. Am J Med Genet A. 2015 Feb;167A(2):407-11. doi: 10.1002/ajmg.a.36842. Epub 2014 ...
    https://medlineplus.gov/genetics/gene/map2k1 - Genetics
  4. Noonan syndrome with multiple lentigines 
    ... novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines. Am J Med Genet A. 2015 Feb;167A(2):407-11. doi: 10.1002/ajmg.a.36842. Epub 2014 ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  5. 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. ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  6. KRAS gene 
    ... Martinez AF, Kruszka P, Muenke M. Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature. Am J Med Genet A. 2015 Nov;167A(11):2657-63. doi: 10.1002/ajmg.a.37259. ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  7. BRAF gene 
    ... Rev Oncol Hematol. 2015 Jul;95(1):1-11. doi: 10.1016/j.critrevonc.2015.02.004. Epub ... Tartaglia M. Noonan Syndrome with Multiple Lentigines. 2007 Nov 30 [updated 2022 ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
  8. Noonan syndrome with multiple lentigines 
    Noonan syndrome with multiple lentigines (NSML) is a rare inherited disorder. People with this condition have problems with ... and heart. The genitals may also be affected. Noonan syndrome with multiple lentigines was formerly known as LEOPARD ...
    https://medlineplus.gov/ency/article/001473.htm - Medical Encyclopedia
  9. Cancer in Children and Adolescents From the National Institutes of Health (National Cancer Institute)  
    Childhood Brain Tumors/Statistics and Research ... Childhood Brain Tumors ... Cancer in Children/Start Here ... Cancer in Children ... Childhood Leukemia/Statistics and Research
    https://www.cancer.gov/.../child-adolescent-cancers-fact-sheet - External Health Links
  10. Neurofibromatosis type 1 
    ... in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS). Am J Med Genet A. 2003 May ... mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome. Am J Hum Genet. 2005 Dec;77(6): ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
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