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Results 1 - 10 of 36 for robert syndrome 10
  1. Roberts syndrome 
    ... 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/condition/roberts-syndrome - Genetics
  2. Warsaw breakage syndrome 
    ... Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome. Anemia. 2010;2010:565268. doi: 10.1155/2010/565268. Epub 2010 Jul 18. Citation ...
    https://medlineplus.gov/genetics/condition/warsaw-breakage-syndrome - Genetics
  3. Noonan syndrome 
    ... 37657. Epub 2016 Apr 25. Citation on PubMed Roberts AE, Allanson JE, Tartaglia M, Gelb BD. Noonan syndrome. Lancet. 2013 Jan 26;381(9863):333-42. doi: 10.1016/S0140-6736(12)61023-X. Epub 2013 ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  4. Short QT syndrome 
    ... 038. Citation on PubMed Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome: proposed diagnostic criteria. J Am Coll Cardiol. 2011 Feb 15;57(7):802-12. doi: 10.1016/j.jacc.2010.09.048. Citation on ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  5. Wolff-Parkinson-White syndrome 
    ... Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N Engl J Med. 2001 Jun 14;344(24):1823-31. doi: 10.1056/NEJM200106143442403. Erratum In: N Engl J Med ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  6. Ehlers-Danlos syndrome 
    ... Frank M, Jeunemaitre X, Johnson D, Pepin M, Robert L, Sanders L, Wheeldon N. Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):40-47. doi: 10.1002/ajmg.c.31553. Citation on PubMed Byers ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  7. Cardiofaciocutaneous syndrome 
    ... a.31315. No abstract available. Citation on PubMed 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. Epub 2006 Jul 6. ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  8. Branchio-oculo-facial syndrome 
    ... on PubMed Milunsky JM, Maher TA, Zhao G, Roberts AE, Stalker HJ, Zori RT, Burch MN, Clemens M, Mulliken JB, Smith R, Lin AE. TFAP2A mutations result in branchio-oculo-facial syndrome. Am J Hum Genet. 2008 May;82(5):1171-7. doi: 10.1016/j.ajhg.2008.03.005. Erratum In: ...
    https://medlineplus.gov/.../condition/branchio-oculo-facial-syndrome - Genetics
  9. 3MC syndrome 
    ... ajmg.a.30878. Citation on PubMed Urquhart J, Roberts R, de ... A. 2016 May;170A(5):1216-24. doi: 10.1002/ajmg.a.37564. Epub 2016 Jan 20. ...
    https://medlineplus.gov/genetics/condition/3mc-syndrome - Genetics
  10. Loeys-Dietz syndrome 
    ... Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco ... doi: 10.1056/NEJMoa055695. Citation on PubMed Luo M, Yang ...
    https://medlineplus.gov/genetics/condition/loeys-dietz-syndrome - Genetics
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