biomedicina slovenica


re="Am J Med Genet" : 11

  1. Dai Nan; Foldager Leslie; Gallego Juan A; Hack Laura M; Ji Yuan; Lett Ttristram A; Liu Bao-Cheng; Loken Erik K; Mandelli Laura; Videtič-Paska Alja
    Summaries from the XIX world congress of psychiatric genetics, Washington, DC, September 10-14, 2011
    2012
  2. Writzl Karin; Lovrečić Luca; Peterlin Borut
    Interstitial deletion 2p11.2-p12: further delineation
    2009
  3. Debeljak Maruša; Zver Aleksandra; Jazbec Janez
    A patient with Baller-Gerold syndrome and midline NK/T lymphoma
    2009
  4. Writzl Karin; Jeruc Jera; Oldridge Michael; Peterlin Borut; Hennekam Raoul C
    Genital anomalies in a patient with Treacher Collins syndrome
    2008
  5. Alkelai A; Baum A; Carless M; Crowley J; Dasbanerjee T; Dempster E; Docherty S; Hare E; Galsworthy MJ; Grover D
    The XVth World Congress of Psychiatric Genetics, October 7-11, 2007: Rapporteur summaries of oral presentations
    2008
  6. Writzl K; Hoovers Jan; Sistermans Erik A; Hennekam Raoul C
    LEOPARD syndrome with partly normal skin and sex chromosome mosaicism
    2007
  7. Dolžan Vita; Kores-Plesničar Blanka; Serretti Alessandro; Mandelli Laura; Zalar bojan; Koprivšek Jure; Breskvar Katja
    Polymorphisms in dopamine receptor DRD1 and DRD2 genes and psychopathological and extrapyramidal symptoms in patients on long-term antipsychotic treatment
    2007
  8. Videtič Alja; Pungerčič Galina; Zupanič-Pajnič Irena; Zupanc Tomaž; Balažic Jože; Tomori Martina; Komel Radovan
    Association study of seven polymorphisms in four serotonin receptor genes on suicide victims
    2006
  9. Marušič Andrej
    History and geography of suicide: could genetic risk factors account for the variation in suicide rates?
    2005
  10. Marčun-Varda Nataša; Kokalj-Vokač N; Kanič Z; Bračič K; Erjavec A; Zagradišnik B; Gregorič A
    Early renal insufficiency in a neonate with de novo partial trisomy of chromosome 10q
    2003
  11. Gabrovšek M; Brecelj-Anderluh M; Bellodi L; Cellini E; Di-Bella D; Estivill X; Fernandez-Aranda F; Freeman B; Komel R; Tomori M
    Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa
    2004


Nova poizvedba      Pripombe      Na vrh strani                        Inštitut za biostatistiko in medicinsko informatiko