Učitavanje...
NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study
BACKGROUND: To determine the carrier frequency and pathogenic variants of common genetic disorders in the north Indian population by using next generation sequencing (NGS). METHODS: After pre-test counselling, 200 unrelated individuals (including 88 couples) were screened for pathogenic variants in...
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| Izdano u: | BMC Med Genet |
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| Glavni autori: | , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7607710/ https://ncbi.nlm.nih.gov/pubmed/33138774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01153-4 |
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