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Results 1 - 10 of 11 for FG syndrome 4
  1. ... recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. Nat Genet. 2007 Apr;39(4):451-3. ... A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome). Clin Genet. 2011 Feb;79(2):183-8. ...
  2. ... on PubMed Toydemir RM, Bamshad MJ. Sheldon-Hall syndrome. Orphanet J Rare Dis. 2009 Mar 23;4:11. doi: 10.1186/1750-1172-4-11. Citation on PubMed or Free article on PubMed Central Toydemir RM, Rutherford A, Whitby FG, Jorde LB, Carey JC, Bamshad MJ. Mutations in ...
  3. ... 26. Erratum In: Nat Genet. 2006 Apr;38(4):495. Kubisch, Chriutian [corrected to ... stature, and hearing loss (CATSHL) syndrome. Am J Hum Genet. 2006 Nov;79(5): ...
  4. ... Gahl WA. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of ... H, Rowley JW, Pluthero FG, Urban D, Fabbro S, Nixon B, Gadzinski R, ...
  5. ... extracellular collagen VI which accumulates in hyaline fibromatosis syndrome. Nat ... Hum Mutat. 2009 Apr;30(4):583-9. doi: 10.1002/humu.20872. Citation ...
  6. ... KH, Angle B, Marmorstein LY, Urban Z. Fibulin-4: a novel gene for an autosomal ... JH, Keene DR, Bachinger HP, Hanisch FG, Markova D, Tsuda T, Timpl R, Chu ML, ...
  7. ... This Health Condition MedlinePlus Genetics provides information about FG ... Feb;1843(2):234-44. doi: 10.1016/j.bbamcr.2013.10.022. Epub 2013 Nov 4. Citation on PubMed or Free article on PubMed ...
  8. ... This Health Condition MedlinePlus Genetics provides information ... and mental retardation. Ann Neurol. 2009 Oct;66(4):438-43. doi: 10.1002/ana.21755. Citation ...
  9. ... Condition MedlinePlus Genetics provides information about Polycystic ... Qiao J, Han B, Liu BL, Chen X, Ru Y, Cheng KX, Chen FG, Zhao SX, Liang J, Lu YL, Tang JF, ...
  10. ... children. Science. 2002 Aug 2;297(5582):851-4. doi: 10.1126/science.1072290. ... into Brunner syndrome and potential for targeted therapy. Clin Genet. 2016 ...
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