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Results 1 - 7 of 7 for Noonan syndrome 5
  1. ... 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 ...
  2. ... Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome patients with RIT1 mutations. Hum Genet. 2016 Feb;135(2):209-22. doi: 10.1007/s00439-015-1627-5. Epub 2015 Dec 29. Citation on PubMed
  3. ... W, Hudgins L. Neonatal pulmonary arterial hypertension and Noonan syndrome: two fatal cases with a specific RAF1 mutation. Am J Med Genet A. 2015 Apr;167A(4):882-5. doi: 10.1002/ajmg.a.37024. Epub 2015 ...
  4. ... Hematol Oncol Clin North Am. 2015 Oct;29(5):839-51. doi: 10.1016/j.hoc.2015.06.004. ... clinical features, diagnosis, and management guidelines. Pediatrics. 2010 ...
  5. ... 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 ...
  6. ... also known as Verma-Naumoff syndrome or Saldino-Noonan syndrome. These disorders have signs and symptoms similar to ... cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III. Am J Hum Genet. 2009 May;84(5):706-11. doi: 10.1016/j.ajhg.2009. ...
  7. ... This Health Condition MedlinePlus Genetics provides information about Noonan syndrome More About This Health Condition Mutations in the ...