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Results 1 - 5 of 5 for Autosomal dominant Robinow syndrome 1
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  1. WNT5A gene 
    ... SC, Lohr JL. WNT5A mutations in patients with autosomal dominant Robinow syndrome. Dev Dyn. 2010 Jan;239(1):327-37. doi: 10.1002/dvdy.22156. Citation ...
    https://medlineplus.gov/genetics/gene/wnt5a - Genetics
  2. DVL1 gene 
    ... HG, Carvalho CMB. DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. Am J Hum Genet. 2016 Mar 3;98( ...
    https://medlineplus.gov/genetics/gene/dvl1 - Genetics
  3. DVL3 gene 
    ... HG, Carvalho CMB. DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. Am J Hum Genet. 2016 Mar 3;98( ...
    https://medlineplus.gov/genetics/gene/dvl3 - Genetics
  4. ROR2 gene 
    ... gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B. Hum Mutat. 2003 Jul;22(1):1-11. doi: 10.1002/humu.10233. Citation ...
    https://medlineplus.gov/genetics/gene/ror2 - Genetics
  5. FZD2 gene 
    ... the FZD2 gene have been found to cause autosomal dominant Robinow syndrome, a condition that affects the development of many ... believe that it actually represents a subtype of autosomal dominant Robinow syndrome.Three of the known mutations change a single ...
    https://medlineplus.gov/genetics/gene/fzd2 - Genetics