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Results 1 - 10 of 13 for Feingold syndrome 2
  1. Feingold syndrome 
    ... 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( ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  2. MIR17HG gene 
    ... Repnikova EA, Amudhavalli SM. Expanding the phenotype of feingold syndrome-2. Am J Med Genet A. 2015 Dec;167A( ... In: Eur J Med Genet. 2014 Feb;57(2-3):123-4. Citation on PubMed ... microRNA action in Feingold syndrome mouse models. Nat Commun. 2018 Apr 10;9( ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
  3. Chromosome 13 
    ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that remove (delete) ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the fingers and ...
    https://medlineplus.gov/genetics/chromosome/13 - Genetics
  4. Weill-Marchesani syndrome 
    ... 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. ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  5. Baller-Gerold syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  6. 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
  7. 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
  8. Meier-Gorlin syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/meier-gorlin-syndrome - Genetics
  9. Vohwinkel syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
  10. ORC6 gene 
    ... cells separate from one another (cytokinesis). At least two mutations in the ORC6 gene have been found ... origin recognition complex formation. Elife. 2013 Oct 8;2:e00882. doi: 10.7554/eLife.00882. Citation on ...
    https://medlineplus.gov/genetics/gene/orc6 - Genetics
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