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Results 1 - 8 of 8 for Fraser syndrome 3
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  1. ... extracellular matrix proteins: structure, function, and association with Fraser syndrome and the mouse bleb phenotype. Connect Tissue Res. 2008;49(3):277-82. doi: 10.1080/03008200802148025. Citation on ...
  2. ... extracellular matrix proteins: structure, function, and association with Fraser syndrome and the mouse bleb phenotype. Connect Tissue Res. 2008;49(3):277-82. doi: 10.1080/03008200802148025. Citation on ...
  3. ... Kayserili H, Satkin BN, Altunoglu U, Zenker M. Fraser syndrome due to mutations in GRIP1--clinical phenotype in two families and expansion of the mutation spectrum. Am J Med Genet A. 2014 Mar;164A(3):837-40. doi: 10.1002/ajmg.a.36343. ...
  4. ... VC, Alward WL. A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by ... R, Ocaka L, Mungall AJ, Fraser S, McGill JI, Hitchings RA, Khaw PT, Sowden ...
  5. ... 10.1002/ajmg.a.37344. Epub 2015 Sep 3. Citation on PubMed Lonie L, Porter DE, Fraser M, Cole T, Wise C, Yates L, Wakeling ... hereditary multiple osteochondromas. Cancer Genet. 2015 Mar;208(3):62-7. doi: ... gene deletion syndrome phenotype: case report and review of the literature. ...
  6. ... pathophysiology of Na(v)1.7-related pain syndromes. Adv Genet. 2008;63:85-110. doi: 10.1016/S0065-2660(08)01004-3. Citation on PubMed Doty CN. SCN9A: another sodium ...
  7. ... failure. Am J Cardiol. 2008 Aug 1;102(3):326-9. doi: 10.1016/j.amjcard.2008.03.063. Epub 2008 May 29. Citation on PubMed Connell JM, Fraser R, MacKenzie SM, Friel EC, Ingram MC, Holloway ...
  8. ... Shimomura Y. GJB6, of which mutations underlie Clouston syndrome, is a ... Christianson AL, Fraser FC, Der Kaloustian VM, Rouleau GA. Clouston hidrotic ...