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Results 1 - 10 of 39 for robert syndrome 10
  1. ESCO2 gene 
    ... ESCO2 expression and establishes the clinical criteria for Roberts syndrome. J Med Genet. 2010 Jan;47(1):30-7. doi: 10.1136/jmg.2009.068395. Epub 2009 Jul 1. ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  2. PRKAG2 gene 
    ... on PubMed Gollob MH, Green MS, Tang AS, Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy. Curr Opin Cardiol. 2002 May;17(3):229-34. doi: 10.1097/00001573-200205000-00004. Citation on PubMed Gollob ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  3. SOS1 gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/sos1 - Genetics
  4. KRAS gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  5. RAF1 gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  6. NRAS gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
  7. BRAF gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/braf - Genetics
  8. PTPN11 gene 
    ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. Epub 2010 Sep 27. ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  9. FTL gene 
    ... Toohey MG, Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA. Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations. Arch Ophthalmol. 2003 Dec;121(12):1753-61. doi: 10.1001/archopht.121.12.1753. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/ftl - Genetics
  10. TNXB gene 
    ... TNXB NCBI Gene ClinVar ... study in 17 patients. Clin Genet. 2017 Mar;91(3):411-425. doi: 10.1111/cge.12853. Epub 2016 Nov 4. Citation ...
    https://medlineplus.gov/genetics/gene/tnxb - Genetics
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