Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Antonia Modelhart"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Genetic diagnosis is often understood as a single event within the care pathway of rare disease patients. Legal, policy and ethical scholarship focusing on rare diseases and genetic information discusses questions of how to best d
Externí odkaz:
https://doaj.org/article/13fb703c998b4e2288ffdebc296a19eb
