Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies

Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies

Background. Intellectual disability affects about 1–2% of the general population worldwide, and this is the leading socio-economic problem of health care. The evaluation of the genetic causes of intellectual disability is challenging because these conditions are genetically heterogeneous with many...

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Bibliographic Details
Main Authors: Eglė Preikšaitienė, Laima Ambrozaitytė, Živilė Maldžienė, Aušra Morkūnienė, Loreta Cimbalistienė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas
Format: Article
Language:English
Published: Vilnius University Press 2016-07-01
Series:Acta Medica Lituanica
Subjects:
intellectual disability
developmental delay
array-CGH
whole exome sequencing
Online Access:https://www.journals.vu.lt/AML/article/view/21439

Internet

https://www.journals.vu.lt/AML/article/view/21439

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