Search Results - "Thongpradit, S"

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals

    High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals by Wattanasirichaigoon, D, Limwongse, C, Jariengprasert, C, Yenchitsomanus, PT, Tocharoenthanaphol, C, Thongnoppakhun, W, Thawil, C, Charoenpipop, D, Pho-iam, T, Thongpradit, S, Duggal, P

    Published in Clinical genetics (01-11-2004)
    “…Hearing loss is highly prevalent with a worldwide incidence of 1–2 per 1000 newborns. Several previous studies have demonstrated that mutations of connexin 26…”
    Get full text
    Journal Article
    Save to List
    Saved in:
  2. 2
    Multiple basal cell nevus syndrome (report of a case)

    Multiple basal cell nevus syndrome (report of a case) by Leelaprute, V, Swasdison, S, Thongpradit, S

    Get more information
    Journal Article
    Save to List
    Saved in:

Search Tools: