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Results 1 - 8 of 8 for Binder syndrome
  1. H19 gene 
    ... Russo S, Said E, Toumba M, Tumer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. Diagnosis and management of Silver-Russell syndrome: first international consensus statement. Nat Rev Endocrinol. 2017 ...
    https://medlineplus.gov/genetics/gene/h19 - Genetics
  2. SHOX gene 
    ... Blaschke RJ, Zuniga A, Zeller R, Robson SC, Binder G, Glass I, Strachan T, Lindsay S, Rappold GA. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum Mol Genet. 2000 Mar 22;9(5): ...
    https://medlineplus.gov/genetics/gene/shox - Genetics
  3. RBM8A gene 
    ... causes the specific signs and symptoms of TAR syndrome. No cases have been reported in which ... binder of OVCA1-1 BOV-1 BOV-1A BOV- ...
    https://medlineplus.gov/genetics/gene/rbm8a - Genetics
  4. TIMM8A gene 
    ... T. Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes. J Hum Genet. 2011 Aug;56(8):577-82. doi: 10.1038/jhg.2011.61. Epub 2011 Jul 14. Citation on PubMed Binder J, Hofmann S, Kreisel S, Wohrle JC, Bazner ...
    https://medlineplus.gov/genetics/gene/timm8a - Genetics
  5. KMT2D gene 
    ... identifies MLL2 mutations as a cause of Kabuki syndrome. Nat Genet. 2010 ... C, Gallia GL, Jallo GI, Binder ZA, Nikolsky Y, Hartigan J, Smith DR, Gerhard ...
    https://medlineplus.gov/genetics/gene/kmt2d - Genetics
  6. NOD2 gene 
    ... S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent- ... factor-kappaB activation: common genetic etiology with Blau syndrome. Blood. 2005 Feb 1;105(3):1195-7. ...
    https://medlineplus.gov/genetics/gene/nod2 - Genetics
  7. CDKN1C gene 
    ... or Free article on PubMed Central Eggermann T, Binder G, Brioude F, Maher ER, Lapunzina P, Cubellis ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  8. MAOA gene 
    ... Hamm A, Kircher T, Arolt V, Wittchen HU, Binder EB, Erhardt A, Deckert J. Meta-analysis argues ... S, Jimbo E, Momoi MY. MAOA/B deletion syndrome in male siblings with severe developmental delay and ...
    https://medlineplus.gov/genetics/gene/maoa - Genetics