Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development.

Autor:	Jespersgaard, Cathrine1 Cathrine.jespersgaard@regionh.dk, Damgaard, Ida N.2, Cornelius, Nanna1, Bache, Iben1,3, Knabe, Niels2, Miranda, Maria J.2, Tümer, Zeynep1
Zdroj:	Molecular Cytogenetics (17558166). 2/4/2016, Vol. 9, p1-7. 7p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu