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

Fuente: Redalyc

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Dettagli Bibliografici
Autore principale:	Eglė Preikšaitienė
Natura:	Artículo científico
Lingua:	en
Pubblicazione:	Vilniaus Universitetas 2016
Soggetti:	Medicina CGH array developmental delay whole exome sequencing Intellectual disability
Accesso online:	Acceder al recurso
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