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Results 1 - 10 of 16 for robert syndrome 22
  1. ... doi: 10.1074/jbc.M207093200. Epub 2002 Oct 22. Citation on PubMed ... for familial Wolff-Parkinson-White syndrome. N Engl J Med. 2001 Jun 14;344( ...
  2. ... ESCO2 gene mutations have been found to cause Roberts syndrome, which is characterized by limb and facial abnormalities ... around the chromosome's constriction point (centromere). In Roberts syndrome, cells respond to abnormal sister chromatid attachment by ...
  3. ... of the disorder. More About This Health Condition 22 kDa FK506-binding protein 22 kDa FKBP EDSKMH FK506 binding protein 14 FK506 binding protein 14, 22 kDa FKBP-22 FKBP22 FLJ20731 IPBP12 peptidyl-prolyl ...
  4. ... translocation) of genetic material between chromosomes 17 and 22. This translocation, written as t(17;22), fuses part of the COL1A1 gene on chromosome ...
  5. ... j.tins.2007.08.004. Epub 2007 Oct 22. Citation on PubMed Dib-Hajj SD, Yang Y, ... doi: 10.1002/ana.22485. Epub 2011 Jun 22. Citation on PubMed Fertleman CR, Ferrie CD, Aicardi ...
  6. ... 3. doi: 10.1038/ng880. Epub 2002 Apr 22. Citation on PubMed Agarwal AK. Lysophospholipid acyltransferases: 1- ... doi: 10.1074/jbc.M509612200. Epub 2006 Feb 22. Citation on PubMed Magre J, Delepine M, Van ...
  7. ... KRAS mutations. Mol Cell Biol. 2007 Nov;27(22):7765-70. doi: 10.1128/MCB.00965-07. ...
  8. ... j.ydbio.2011.09.019. Epub 2011 Sep 22. Citation on PubMed or Free article on PubMed ...
  9. ... 1007/s00018-015-1880-8. Epub 2015 Mar 22. Citation on PubMed
  10. ... peculiar form of distal myopathy. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl. ...
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