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Results 1 - 6 of 6 for Feingold syndrome 2
  1. ... for Rare Disorders (NORD) FEINGOLD SYNDROME 1; FGLDS1 FEINGOLD SYNDROME 2; FGLDS2 PubMed Celli J, van Bokhoven H, Brunner ... Repnikova EA, Amudhavalli SM. Expanding the phenotype of feingold syndrome-2. Am J Med Genet A. 2015 Dec;167A( ...
  2. ... Megarbane A, Samples J, Gorlin RJ, Alswaid A, Feingold J, Le Merrer M, Munnich A, Cormier-Daire V. Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome. Am J Med Genet A. 2003 Dec 1;123A(2):204-7. doi: 10.1002/ajmg.a.20289. ...
  3. ... Bloom AD. Baller-Gerold syndrome craniosynostosis-radial aplasia syndrome. Clin Genet. 1980 Feb;17(2):161-6. doi: 10.1111/j.1399-0004.1980.tb00126.x. Citation on PubMed Feingold M, Sklower SL, Willner JP, Desnick RH, Cohen ...
  4. ... MEIER-GORLIN SYNDROME 1; MGORS1 MEIER-GORLIN SYNDROME 2; MGORS2 MEIER-GORLIN SYNDROME 3; MGORS3 ... S, Al-Aama JY, Bober M, Brown PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers ...
  5. ... for making a protein called gap junction beta 2, more commonly known as connexin 26. Connexin 26 ... J Hand Surg Eur Vol. 2009 Apr;34(2):235-7. doi: 10.1177/1753193408098901. Epub 2009 ...
  6. ... foot-genital syndrome. Nat Genet. 1997 Feb;15(2):179-80. doi: 10.1038/ng0297-179. Citation ...