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Results 1 - 10 of 45 for Classical article
  1. Hodgkin lymphoma in children 
    ... system protects us against diseases and infections. This article is about classical Hodgkin lymphoma in children, the most common type.
    https://medlineplus.gov/ency/article/007685.htm - Medical Encyclopedia
  2. Types of OI (Osteogenesis Imperfecta Foundation)  
    Osteogenesis Imperfecta/Specifics ... Osteogenesis Imperfecta ... Osteogenesis Imperfecta Foundation
    https://oif.org/informationcenter/about-oi - External Health Links
  3. COL5A1 gene 
    ... haploinsufficiency is a common molecular mechanism underlying the classical form of EDS. Am J Hum Genet. 2000 Jun;66(6):1766-76. doi: 10.1086/302930. Epub 2000 Apr 24. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/col5a1 - Genetics
  4. Hereditary xanthinuria 
    ... mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria. J Clin Invest. 1997 May 15;99(10):2391-7. doi: 10.1172/JCI119421. Citation on PubMed or Free article on PubMed Central Ichida K, Amaya Y, Okamoto ...
    https://medlineplus.gov/genetics/condition/hereditary-xanthinuria - Genetics
  5. XDH gene 
    ... mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria. J Clin Invest. 1997 May 15;99(10):2391-7. doi: 10.1172/JCI119421. Citation on PubMed or Free article on PubMed Central Ichida K, Amaya Y, Noda ...
    https://medlineplus.gov/genetics/gene/xdh - Genetics
  6. Mucolipidosis III alpha/beta 
    ... 2009 Jul 16. Citation on PubMed or Free article on PubMed Central Kudo M, Brem MS, Canfield WM. Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in ...
    https://medlineplus.gov/.../condition/mucolipidosis-iii-alpha-beta - Genetics
  7. Mucolipidosis II alpha/beta 
    ... 2009 Jul 16. Citation on PubMed or Free article on PubMed Central Kudo M, Brem MS, Canfield WM. Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in ...
    https://medlineplus.gov/.../condition/mucolipidosis-ii-alpha-beta - Genetics
  8. GNPTAB gene 
    ... 2009 Jul 16. Citation on PubMed or Free article on PubMed Central Kudo M, Brem MS, Canfield WM. Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in ...
    https://medlineplus.gov/genetics/gene/gnptab - Genetics
  9. ATP7A gene 
    ... of the ATP7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndrome. Am J Hum Genet. 2000 Apr;66(4):1211-20. doi: 10.1086/302857. Epub 2000 Mar 17. Citation on PubMed or Free article on PubMed Central Prohaska JR. Role of copper ...
    https://medlineplus.gov/genetics/gene/atp7a - Genetics
  10. Miller-Dieker syndrome 
    ... MDLS PubMed Allanson JE, Ledbetter DH, Dobyns WB. Classical lissencephaly syndromes: does the face reflect the brain? J Med Genet. 1998 Nov;35(11):920-3. doi: 10.1136/jmg.35.11.920. Citation on PubMed or Free article on PubMed Central Cardoso C, Leventer RJ, Ward ...
    https://medlineplus.gov/genetics/condition/miller-dieker-syndrome - Genetics
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