Á lódáil...
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...
Na minha lista:
| Foilsithe in: | Ann Pediatr Endocrinol Metab |
|---|---|
| Main Authors: | , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
The Korean Society of Pediatric Endocrinology
2017
|
| Ábhair: | |
| Rochtain Ar Líne: | 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 |
| Clibeanna: |
Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!
|