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Results 1 - 10 of 54 for mclean
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  1. KRT17 gene 
    ... Paller AS, Munro CS, Jonkman MF, Uitto J, McLean WH. Keratin 17 mutations cause either steatocystoma multiplex ... Bayliss SJ, Uliana V, Fimiani M, Lane EB, McLean WH, Leachman SA, Smith FJ. A spectrum of ...
    https://medlineplus.gov/genetics/gene/krt17 - Genetics
  2. X-linked infantile nystagmus 
    ... GDE, Han J, Kessel L, van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov ... Thomas S, Shah N, Proudlock FA, Thompson JR, McLean RJ, Degg C, Woodruff G, Gottlob I. The ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  3. KRT16 gene 
    ... on PubMed or Free article on PubMed Central McLean WH, Hansen CD, Eliason MJ, Smith FJ. The ... 59. Epub 2011 Mar 24. Citation on PubMed McLean WH, Rugg EL, Lunny DP, Morley SM, Lane ...
    https://medlineplus.gov/genetics/gene/krt16 - Genetics
  4. Pachyonychia congenita 
    ... 009. Epub 2012 Jan 20. Citation on PubMed McLean WH, Hansen CD, Eliason MJ, Smith FJ. The ... Pals G, Collins P, Leachman SA, Munro CS, McLean WH. The genetic basis of pachyonychia congenita. J ...
    https://medlineplus.gov/genetics/condition/pachyonychia-congenita - Genetics
  5. FLG gene 
    ... FLG ICHTHYOSIS VULGARIS NCBI Gene ClinVar Brown SJ, McLean WH. One remarkable molecule: filaggrin. J Invest Dermatol. ... or Free article on PubMed Central Irvine AD, McLean WH, Leung DY. Filaggrin mutations associated with skin ...
    https://medlineplus.gov/genetics/gene/flg - Genetics
  6. KRT6A gene 
    ... Bayliss SJ, Uliana V, Fimiani M, Lane EB, McLean WH, Leachman SA, Smith FJ. A spectrum of ... 003. Epub 2007 Aug 24. Citation on PubMed McLean WH, Hansen CD, Eliason MJ, Smith FJ. The ...
    https://medlineplus.gov/genetics/gene/krt6a - Genetics
  7. Steatocystoma multiplex 
    ... Paller AS, Munro CS, Jonkman MF, Uitto J, McLean WH. Keratin 17 mutations cause either steatocystoma multiplex ... Gass JK, Wilson NJ, Smith FJ, Lane EB, McLean WH, Rytina E, Salvary I, Burrows NP. Steatocystoma ...
    https://medlineplus.gov/genetics/condition/steatocystoma-multiplex - Genetics
  8. KRT6B gene 
    ... KERATIN 6B, TYPE II; KRT6B NCBI Gene ClinVar McLean WH, Hansen CD, Eliason MJ, Smith FJ. The ... Goor H, Coleman CM, Covello SP, Uitto J, McLean WH. A mutation in human keratin K6b produces ...
    https://medlineplus.gov/genetics/gene/krt6b - Genetics
  9. Cap myopathy 
    ... Clarke NF, Domazetovska A, Waddell L, Kornberg A, McLean C, North KN. Cap disease due to mutation ... Waddell LB, Kreissl M, Kornberg A, Kennedy P, McLean C, Labarre-Vila A, Monnier N, North KN, ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
  10. KRT6C gene 
    ... AG, Leachman SA, O'Toole EA, Lane EB, McLean WH, Smith FJ. Keratin K6c mutations cause focal ... CD, Shepherd AA, Al-Asadi E, Schwartz ME, McLean WH, Sprecher E, Smith FJ. The molecular genetic ...
    https://medlineplus.gov/genetics/gene/krt6c - Genetics
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