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Results 1 - 10 of 10 for Feingold syndrome
  1. MYCN gene 
    ... the MYCN gene have been found to cause Feingold syndrome type 1. This developmental disorder is characterized by ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. ...
    https://medlineplus.gov/genetics/gene/mycn - Genetics
  2. MIR17HG gene 
    ... reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by ... the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  3. LORICRIN gene 
    ... Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122( ...
    https://medlineplus.gov/genetics/gene/loricrin - Genetics
  4. HOXA13 gene 
    ... Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Am J Hum Genet. 2000 Jul;67(1): ...
    https://medlineplus.gov/genetics/gene/hoxa13 - Genetics
  5. ORC1 gene 
    ... PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers NV, Mackenzie J, Opitz JM, Sarda P, Ross A, Temple IK, Toutain A, Wise CA, Wright M, Jackson AP. Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):356- ...
    https://medlineplus.gov/genetics/gene/orc1 - Genetics
  6. CDC6 gene 
    ... PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers NV, Mackenzie J, Opitz JM, Sarda P, Ross A, Temple IK, Toutain A, Wise CA, Wright M, Jackson AP. Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):356- ...
    https://medlineplus.gov/genetics/gene/cdc6 - Genetics
  7. ORC4 gene 
    ... PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers NV, Mackenzie J, Opitz JM, Sarda P, Ross A, Temple IK, Toutain A, Wise CA, Wright M, Jackson AP. Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):356- ...
    https://medlineplus.gov/genetics/gene/orc4 - Genetics
  8. ORC6 gene 
    ... PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers NV, Mackenzie J, Opitz JM, Sarda P, Ross A, Temple IK, Toutain A, Wise CA, Wright M, Jackson AP. Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):356- ...
    https://medlineplus.gov/genetics/gene/orc6 - Genetics
  9. CDT1 gene 
    ... PA, van Bokhoven H, Dean J, Edrees AY, Feingold M, Fryer A, Hoefsloot LH, Kau N, Knoers NV, Mackenzie J, Opitz JM, Sarda P, Ross A, Temple IK, Toutain A, Wise CA, Wright M, Jackson AP. Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nat Genet. 2011 Feb 27;43(4):356- ...
    https://medlineplus.gov/genetics/gene/cdt1 - Genetics
  10. IRF6 gene 
    ... IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet. 2002 Oct;32(2):285-9. doi: 10.1038/ng985. Epub 2002 Sep 3. Citation on PubMed or Free article on PubMed Central Mukhopadhyay N, Feingold E, Moreno-Uribe L, Wehby G, Valencia-Ramirez ...
    https://medlineplus.gov/genetics/gene/irf6 - Genetics