Search Results - "Intarak, N"

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  1. 1
    A novel PITX2 mutation in non‐syndromic orodental anomalies

    A novel PITX2 mutation in non‐syndromic orodental anomalies by Intarak, N, Theerapanon, T, Ittiwut, C, Suphapeetiporn, K, Porntaveetus, T, Shotelersuk, V

    Published in Oral diseases (01-05-2018)
    “…Objective To identify orodental characteristics and genetic aetiology of a family affected with non‐syndromic orodental anomalies. Subjects and Methods…”
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  2. 2
    Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

    Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia by Intarak, N., Theerapanon, T., Srijunbarl, A., Suphapeetiporn, K., Porntaveetus, T., Shotelersuk, V.

    Published in British journal of dermatology (1951) (01-09-2018)
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  3. 3
    Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

    Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia by Intarak, N, Theerapanon, T, Srijunbarl, A, Suphapeetiporn, K, Porntaveetus, T, Shotelersuk, V

    Published in The British journal of dermatology (01-09-2018)
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