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Results 1 - 10 of 31 for robert syndrome 20
  1. ... ajmg.a.30878. Citation on PubMed Urquhart J, Roberts R, de Silva ... Jan 20. Citation on PubMed Venkatraman Girija U, Furze CM, ...
  2. ... Twinkle)-linked adPEO. Neurology. 2010 May 18;74(20):1619-26. doi: 10.1212/WNL.0b013e3181df099f. Citation ... 10.1074/jbc.M110.151795. Epub 2010 Jul 20. Citation on PubMed or Free article on PubMed ...
  3. ... on PubMed Gollob MH, Green MS, Tang AS, Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac ...
  4. ... as many as 1 in 5,000 to 20,000 people, while the classical type probably occurs in 1 in 20,000 to 40,000 people. Other forms of ... Variants (also known as mutations) in at least 20 genes have been found to cause the Ehlers- ...
  5. ... The cause of Noonan syndrome in 15 to 20 percent of people with this disorder is unknown. ... 10.1136/jmedgenet-2015-103018. Epub 2015 Mar 20. Citation on PubMed
  6. ... j.nmd.2009.08.015. Epub 2009 Sep 20. Citation on PubMed Gazzerro E, Bonetto A, Minetti ... long-QT syndrome. Circulation. 2006 Nov 14;114(20):2104-12. doi: 10.1161/CIRCULATIONAHA.106.635268. ...
  7. ... to spread across the muscle, lasting 5 to 20 seconds. A bump or other sudden impact on ... disease. Ann Neurol. 2003 Apr;53(4):512-20. doi: 10.1002/ana.10501. Citation on PubMed ...
  8. ... region of chromosome 14 called 14q32 occurs in 20 to 60 percent of cases of multiple myeloma, ... review. Pediatr Neurol. 2005 Feb;32(2):116-20. doi: 10.1016/j.pediatrneurol.2004.07.007. ...
  9. ... I deficiency More About This Health Condition About 20 mutations in the MT-TL1 gene have been ... Sci U S A. 2005 May 17;102(20):7127-32. doi: 10.1073/pnas.0500563102. Epub ...
  10. ... 10.1136/jmg.2006.046300. Epub 2006 Oct 20. Citation on PubMed or Free article on PubMed ...
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