Displaying all 5 publications

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  1. KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr)
    Tang MM, Surana U, Leong KF, Pramano ZAD
    Int J Dermatol, 2021 Jul;60(7):e288-e290.
    PMID: 33728648 DOI: 10.1111/ijd.15523
    Matched MeSH terms: Ichthyosis*
  2. Perspectives in dermatology: Malaysia
    Petit JH
    Int J Dermatol, 1976 Sep;15(7):505-12.
    PMID: 965135
    Matched MeSH terms: Ichthyosis/epidemiology
  3. Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia
    Numata S, Teye K, Krol RP, Karashima T, Fukuda S, Matsuda M, et al.
    J. Dermatol. Sci., 2015 Apr;78(1):82-5.
    PMID: 25766764 DOI: 10.1016/j.jdermsci.2015.02.006
    Matched MeSH terms: Ichthyosis, Lamellar/diagnosis; Ichthyosis, Lamellar/ethnology; Ichthyosis, Lamellar/genetics*
  4. Foetal itchyosis. Harlequin foetus
    Hewitson M
    Malayan Medical Journal, 1932;7:93.
    Matched MeSH terms: Ichthyosis
  5. Two interesting skin conditions in children
    PAUL FM
    Med J Malaya, 1958 Mar;12(3):540-5.
    PMID: 13565025
    Matched MeSH terms: Ichthyosis*; Ichthyosis, Lamellar*
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