biomedicina slovenica


pr=Alazami : 2

  1. Alazami Anas M.; Kojović Maja
    C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
    2010
  2. Alazami Anas M; Al-Saif Amr; Al-Semari Abdulaziz; Bohlega Saeed; Zlitni Soumaya; Alzahrani Fatema; Bavi Prashant; Kaya Namik; Colak Dilek; Peterlin Borut
    Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
    2008


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