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Changing trends in carrier screening for genetic disease in the United States
Genetic disease is the leading cause of infant death in the United States, accounting for approximately 20% of annual infant mortality. Advances in genomic medicine and technological platforms have made possible low cost, pan‐ethnic expanded genetic screening that enables obstetric care providers to...
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| 出版年: | Prenat Diagn |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4758394/ https://ncbi.nlm.nih.gov/pubmed/26138560 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pd.4647 |
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