Causal Genetic Variants in Stillbirth

BACKGROUND: In the majority of cases, the cause of stillbirth remains unknown despite detailed clinical and laboratory evaluation. Approximately 10 to 20% of stillbirths are attributed to chromosomal abnormalities. However, the causal nature of single-nucleotide variants and small insertions and del...

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Detaylı Bibliyografya
Yayımlandı:N Engl J Med
Asıl Yazarlar: Stanley, K.E., Giordano, J., Thorsten, V., Buchovecky, C., Thomas, A., Ganapathi, M., Liao, J., Dharmadhikari, A.V., Revah‑Politi, A., Ernst, M., Lippa, N., Holmes, H., Povysil, G., Hostyk, J., Parker, C.B., Goldenberg, R., Saade, G.R., Dudley, D.J., Pinar, H., Hogue, C., Reddy, U.M., Silver, R.M., Aggarwal, V., Allen, A.S., Wapner, R.J., Goldstein, D.B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2020
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7604888/
https://ncbi.nlm.nih.gov/pubmed/32786180
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJMoa1908753
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