De novo 393kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features

Author:

Varvagiannis Konstantinos,Papoulidis Ioannis,Koromila Theodora,Kefalas Konstantinos,Ziegler Monika,Liehr Thomas,Petersen Michael B.,Gyftodimou Yolanda,Manolakos Emmanouil

Funder

European Commission

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference38 articles.

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