Zobrazeno 1 - 2
of 2
pro vyhledávání: '"bisfosfonatei"'
Publikováno v:
Paediatria Croatica
Volume 61
Issue 3
Volume 61
Issue 3
Osteogenesis imperfecta (OI) je fenotipski i molekularno heterogena skupina nasljednih bolesti veziva obilježena smanjenom gustoćom kostiju, čestim lomovima i deformacijama. Većina OI-a nasljeđuje se autosomno dominantno i uzrokovana je mutacija
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cd02efb653c4863474daa8647ab1e9a3
https://www.bib.irb.hr/1063839
https://www.bib.irb.hr/1063839
Publikováno v:
Paediatria Croatica
Volume 61
Issue 3
Volume 61
Issue 3
Osteogenesis imperfecta (OI) is a phenotypically and molecularly heterogeneous group of heritable connective tissue disorders characterized by low bone mineral density, recurrent fractures, and bone deformities. Most cases of OI are inherited in an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::f7ed976e8afd522bd945ad4c74e4a2fa
https://hrcak.srce.hr/201163
https://hrcak.srce.hr/201163
