Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3

Chromosome 17p13.3 is a region of genomic instability that is linked to different rare neurodevelopmental genetic diseases, depending on whether a deletion or duplication of the region has occurred. Chromosome microdeletions within 17p13.3 can result in either isolated lissencephaly sequence (ILS) o...

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Detalles Bibliográficos
Autores principales: Blazejewski, Sara M., Bennison, Sarah A., Smith, Trevor H., Toyo-oka, Kazuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876250/
https://www.ncbi.nlm.nih.gov/pubmed/29628935
http://dx.doi.org/10.3389/fgene.2018.00080

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876250/
https://www.ncbi.nlm.nih.gov/pubmed/29628935
http://dx.doi.org/10.3389/fgene.2018.00080

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