All Stories

  1. Thiamine responsive megaloblastic anemia syndrome: A novel homozygousSLC19A2gene mutation identified

    Article • American Journal of Medical Genetics Part A, February 2015, Wiley

    Mrs Violeta Mikstiene

  2. Hereditary hearing loss. Genetic factors in ethiopathogenesis of deafness

    Article • Medicinos teorija ir praktika, December 2014, Medicinos Mintis

    Mrs Violeta Mikstiene