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Results 1 - 10 of 12 for robert syndrome 22
  1. Branchio-oculo-facial syndrome 
    ... Mortier GR, Parkash S, Ray CR, Roberts A, Roberts A, Reardon W, Schnur RE, Smith R, Splitt M, Tezcan K, Whiteford ML, Wong DA, Zori R, Lin AE. Genotype-phenotype analysis of the branchio-oculo-facial syndrome. Am J Med Genet A. 2011 Jan;155A(1):22-32. doi: 10.1002/ajmg.a.33783. Citation ...
    https://medlineplus.gov/.../condition/branchio-oculo-facial-syndrome - Genetics
  2. Roberts syndrome 
    Roberts syndrome is a genetic disorder characterized by limb and facial abnormalities. Affected individuals also grow slowly before and after birth. Mild to ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  3. Noonan syndrome 
    ... 7. doi: 10.1159/000243772. Epub 2009 Dec 22. Citation on PubMed Romano AA, Allanson JE, 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 ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  4. Ehlers-Danlos syndrome 
    ... Hakim A. Hypermobile Ehlers-Danlos Syndrome. 2004 Oct 22 [updated 2024 Feb 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, Sobey ... of the Ehlers-Danlos syndromes. Am J Med Genet C Semin Med Genet. ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  5. Short QT syndrome 
    ... Dumaine R. Short QT syndrome. CMAJ. 2005 Nov 22;173(11):1349-54. doi: 10.1503/cmaj. ... 038. Citation on PubMed Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome: proposed diagnostic criteria. J Am Coll Cardiol. 2011 ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  6. Restless legs syndrome 
    ... cases. Arch Neurol. 2010 May;67(5):617-22. doi: 10.1001/archneurol.2010.67. Citation on ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
  7. Neuropathy, ataxia, and retinitis pigmentosa 
    ... Neurol Neurosurg Psychiatry. 1997 Jul;63(1):16-22. doi: 10.1136/jnnp.63.1.16. Citation ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  8. FOXP2-related speech and language disorder 
    ... 80. doi: 10.1086/430841. Epub 2005 Apr 22. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  9. 16p11.2 deletion syndrome 
    ... Chung W. 16p11.2 Recurrent Deletion. 2009 Sep 22 [updated 2021 Oct 28]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  10. Autosomal recessive primary microcephaly 
    ... microcephaly due to ASPM mutations. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL. ...
    https://medlineplus.gov/.../autosomal-recessive-primary-microcephaly - Genetics
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