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Results 1 - 6 of 6 for Reynolds syndrome
  1. SLC26A4 gene 
    ... Zalewski CK, Muskett J, Chattaraj P, Shawker T, Reynolds JC, Butman JA, Brewer CC, ... Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  2. CDH23 gene 
    ... mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. J Med Genet. 2011 Nov;48(11):767-75. doi: 10.1136/jmedgenet-2011-100262. Epub 2011 Sep 22. Citation on PubMed Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, Gillespie PG, Muller U. Cadherin ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  3. WASHC5 gene 
    ... b. Citation on PubMed Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  4. ERCC2 gene 
    ... Xiong M, Tamura D, Khan SG, Rizza ERH, Reynolds JC, Paul SM, Hill SC, Kraemer KH. Debilitating ... MW. Xeroderma pigmentosum: its overlap with trichothiodystrophy, Cockayne syndrome and other progeroid syndromes. Adv Exp Med Biol. ...
    https://medlineplus.gov/genetics/gene/ercc2 - Genetics
  5. CFI gene 
    ... PubMed Central Fagerness JA, Maller JB, Neale BM, Reynolds RC, Daly MJ, Seddon JM. Variation near complement ... complement factor I (CFI) associated with hemolytic uremic syndrome. Mol Immunol. 2008 Jan;45(1):95-105. ...
    https://medlineplus.gov/genetics/gene/cfi - Genetics
  6. CARD11 gene 
    ... Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal ...
    https://medlineplus.gov/genetics/gene/card11 - Genetics