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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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| Vydáno v: | Ann Pediatr Endocrinol Metab |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Korean Society of Pediatric Endocrinology
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5495984/ https://ncbi.nlm.nih.gov/pubmed/28690986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2017.22.2.90 |
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