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Results 1 - 10 of 20 for Steel syndrome
  1. Ornithine translocase deficiency 
    ... Biery B, Goodman BK, Hu CA, Almashanu S, Steel G, Casey R, Lambert M, Mitchell GA, Valle D. Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  2. SLC25A15 gene 
    ... Biery B, Goodman BK, Hu CA, Almashanu S, Steel G, Casey R, Lambert M, Mitchell GA, Valle D. Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics
  3. Kaufman oculocerebrofacial syndrome 
    ... Kelley RI, Shohat M, Nurnberg P, Flint J, Steel KP, Hoppe T, Kubisch C, Adams DJ, Borck G. Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome. Am J Hum Genet. 2012 Dec 7;91( ...
    https://medlineplus.gov/.../kaufman-oculocerebrofacial-syndrome - Genetics
  4. UBE3B gene 
    ... Kelley RI, Shohat M, Nurnberg P, Flint J, Steel KP, Hoppe T, Kubisch C, Adams DJ, Borck G. Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome. Am J Hum Genet. 2012 Dec 7;91( ...
    https://medlineplus.gov/genetics/gene/ube3b - Genetics
  5. MYO7A gene 
    ... history and retinal structure in patients with Usher syndrome type 1 owing to ... P, Kendrick-Jones J, Cope MJ, Steel KP, Brown SD. Mutations in the myosin VIIA ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  6. Hexavalent Chromium From the National Institutes of Health (National Institute of Environmental Health Sciences)  
    Environmental Health/Specifics ... Environmental Health ... National Institute of Environmental Health Sciences ... Hexavalent chromium is a form of the metallic element ...
    https://www.niehs.nih.gov/health/topics/agents/hex-chromium - External Health Links
  7. PRODH gene 
    ... PRODH NCBI Gene ClinVar Bender HU, Almashanu S, Steel G, Hu CA, Lin WW, Willis A, Pulver ... Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome. J Inherit Metab Dis. 2000 Dec;23(8): ...
    https://medlineplus.gov/genetics/gene/prodh - Genetics
  8. Piebaldism 
    ... al. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism. Am J ... ep12399455. Citation on PubMed Spritz RA. Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development. Semin Cutan ...
    https://medlineplus.gov/genetics/condition/piebaldism - Genetics
  9. Problems of the Digestive System (American College of Obstetricians and Gynecologists)  
    Most common digestive problems are short term and easy to control with lifestyle changes and sometimes medication. In some cases, these problems can be ...
    https://www.acog.org/.../faqs/problems-of-the-digestive-system - External Health Links
  10. KIT gene 
    ... al. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism. Am J ... ep12399455. Citation on PubMed Spritz RA. Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development. Semin Cutan ...
    https://medlineplus.gov/genetics/gene/kit - Genetics
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