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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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| Yayımlandı: | Ann Pediatr Endocrinol Metab |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Korean Society of Pediatric Endocrinology
2017
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| Konular: | |
| Online Erişim: | 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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