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Results 1 - 10 of 43 for Chitayat syndrome
  1. Bunion 
    ... rare genetic syndromes that affect bone development, including Chitayat syndrome and fibrodysplasia ossificans progressiva. Bunions are a complex ...
    https://medlineplus.gov/genetics/condition/bunion - Genetics
  2. Robinow syndrome 
    ... Roifman M, Brunner H, Lohr J, Mazzeu J, Chitayat D. Autosomal Dominant Robinow Syndrome. 2015 Jan 8 [updated 2019 Oct 3]. In: ... B, Seaward G; FORGE Canada Consortium; Brunner HG, Chitayat D. De novo ... syndrome suggests specificity of genotype and phenotype. Clin Genet. ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  3. Capillary malformation-arteriovenous malformation syndrome 
    ... Hest L, Vaux KK, Vicente A, Weibel L, Chitayat D, Vikkula M. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast- ...
    https://medlineplus.gov/...ation-arteriovenous-malformation-syndrome - Genetics
  4. RASA1 gene 
    ... Hest L, Vaux KK, Vicente A, Weibel L, Chitayat D, Vikkula M. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast- ...
    https://medlineplus.gov/genetics/gene/rasa1 - Genetics
  5. Parkes Weber syndrome 
    ... Hest L, Vaux KK, Vicente A, Weibel L, Chitayat D, Vikkula M. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast- ...
    https://medlineplus.gov/genetics/condition/parkes-weber-syndrome - Genetics
  6. WNT5A gene 
    ... B, Seaward G; FORGE Canada Consortium; Brunner HG, Chitayat D. De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Clin Genet. ...
    https://medlineplus.gov/genetics/gene/wnt5a - Genetics
  7. MID1 gene 
    ... Dennis N, Odent S, Rastogi A, Liebelt J, Chitayat D, Winter R, Jawanda H, Ballabio A, Franco B, Meroni G. X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition ...
    https://medlineplus.gov/genetics/gene/mid1 - Genetics
  8. Opitz G/BBB syndrome 
    ... Dennis N, Odent S, Rastogi A, Liebelt J, Chitayat D, Winter R, Jawanda H, Ballabio A, Franco B, Meroni G. X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  9. Weaver syndrome 
    ... R, An J, Marra MA; FORGE Canada Consortium; Chitayat D, Boycott KM, Weaver DD, Jones SJ. Mutations in EZH2 cause Weaver syndrome. Am J Hum Genet. 2012 Jan 13;90( ...
    https://medlineplus.gov/genetics/condition/weaver-syndrome - Genetics
  10. EZH2 gene 
    ... R, An J, Marra MA; FORGE Canada Consortium; Chitayat D, Boycott KM, Weaver DD, Jones SJ. Mutations in EZH2 cause Weaver syndrome. Am J Hum Genet. 2012 Jan 13;90( ...
    https://medlineplus.gov/genetics/gene/ezh2 - Genetics
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