Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders

Next-generation sequencing (NGS) and array-based comparative genomic hybridization (array CGH) have enabled us to perform high-throughput mutation screening and genome-wide copy number analysis, respectively. These methods can be used for molecular diagnosis of pediatric endocrine disorders. NGS has...

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Detalles Bibliográficos
Autores principales: Fukami, Maki, Miyado, Mami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495984/
https://www.ncbi.nlm.nih.gov/pubmed/28690986
http://dx.doi.org/10.6065/apem.2017.22.2.90

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495984/
https://www.ncbi.nlm.nih.gov/pubmed/28690986
http://dx.doi.org/10.6065/apem.2017.22.2.90

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