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Screening for fetal chromosomal and subchromosomal disorders
Screening for fetal chromosomal disorders has evolved greatly over the last four decades. Initially, only maternal age-related risks of aneuploidy were provided to patients. This was followed by screening with maternal serum analytes and ultrasound markers, followed by the introduction and rapid upt...
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| 出版年: | Semin Fetal Neonatal Med |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5891357/ https://ncbi.nlm.nih.gov/pubmed/29128491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.siny.2017.10.006 |
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