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Results 1 - 10 of 79 for EC 23
  1. Congenital fibrosis of the extraocular muscles 
    ... 04-1125. Citation on PubMed Heidary G, Engle EC, Hunter DG. Congenital fibrosis of the extraocular muscles. Semin Ophthalmol. 2008 Jan-Feb;23(1):3-8. doi: 10.1080/08820530701745181. Citation ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  2. PHOX2A gene 
    ... Free article on PubMed Central Heidary G, Engle EC, Hunter DG. Congenital fibrosis of the extraocular muscles. Semin Ophthalmol. 2008 Jan-Feb;23(1):3-8. doi: 10.1080/08820530701745181. Citation ...
    https://medlineplus.gov/genetics/gene/phox2a - Genetics
  3. SLC16A2 gene 
    ... Pract Endocrinol Metab. 2006 Sep;2(9):512-23. doi: 10.1038/ncpendmet0262. Citation on PubMed Friesema EC, Kuiper GG, Jansen J, Visser TJ, Kester MH. ...
    https://medlineplus.gov/genetics/gene/slc16a2 - Genetics
  4. Clinical Screening and Diagnosis for Hepatitis C (Centers for Disease Control and Prevention)  
    Check CDC & USPSTF guidelines for hepatitis C screening among adults and the testing sequence. ... Health Screening/Specifics ... Health Screening ... Centers for Disease ...
    https://www.cdc.gov/hepatitis-c/hcp/diagnosis-testing - External Health Links
  5. Arginine vasopressin deficiency 
    ... Jul;7(7):G8-G11. doi: 10.1530/EC-18-0154. Citation on PubMed Christensen JH, Rittig S. Familial neurohypophyseal diabetes insipidus--an update. Semin Nephrol. 2006 May;26(3):209-23. doi: 10.1016/j.semnephrol.2006.03.003. ...
    https://medlineplus.gov/.../arginine-vasopressin-deficiency - Genetics
  6. FBLN5 gene 
    ... De Paepe A, Mecham RP, Choi J, Davis EC, Urban Z. Fibulin-5 mutations: mechanisms of impaired elastic fiber formation in recessive cutis laxa. Hum Mol Genet. 2006 Dec 1;15(23):3379-86. doi: 10.1093/hmg/ddl414. Epub ...
    https://medlineplus.gov/genetics/gene/fbln5 - Genetics
  7. 46,XX testicular difference of sex development 
    ... In: Hum Mol Genet. 2016 Dec 1;25(23):5286. doi: 10.1093/hmg/ddw390. Citation on PubMed Delot EC, Vilain EJ. Nonsyndromic 46,XX Testicular Disorders/Differences ...
    https://medlineplus.gov/...-testicular-difference-of-sex-development - Genetics
  8. Depression 
    ... PubMed or Free article on PubMed Central Dunn EC, Brown RC, Dai Y, Rosand J, Nugent NR, Amstadter AB, Smoller JW. Genetic determinants of depression: recent findings and future directions. Harv Rev Psychiatry. 2015 Jan-Feb;23(1):1-18. doi: 10.1097/HRP.0000000000000054. ...
    https://medlineplus.gov/genetics/condition/depression - Genetics
  9. FBN1 gene 
    ... De Paepe A, Judge DP, Wigley F, Davis EC, Mardon HJ, Handford P, Keene DR, Sakai LY, Dietz HC. Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome. Sci Transl Med. 2010 Mar 17;2(23):23ra20. doi: 10.1126/scitranslmed.3000488. Citation on ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
  10. KIF21A gene 
    ... Patney S, Vogel MC, Rizzo JF 3rd, Engle EC. Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3). Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23. doi: 10.1167/iovs.03-1413. Citation on ...
    https://medlineplus.gov/genetics/gene/kif21a - Genetics
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