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Results 1 - 10 of 19 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. Chromium From the National Institutes of Health (National Institutes of Health, Office of Dietary Supplements)  
    ... meat depends on the animal’s diet. Using stainless steel equipment to process or cook foods can increase ... improve blood sugar control in some people. Metabolic syndrome Metabolic syndrome—the combination of excess belly fat, ...
    https://ods.od.nih.gov/factsheets/Chromium-Consumer - Drugs and Supplements
  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)  
    Digestive Diseases/Start Here ... Digestive Diseases ... American College of Obstetricians and Gynecologists ... Most common digestive problems are short term and easy ...
    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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