Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study-Reference-Cited by-同舟云学术

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Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study

Published:2024-05-30 Issue:2 Volume:310 Page:933-942
ISSN:1432-0711
Container-title:Archives of Gynecology and Obstetrics
language:en
Short-container-title:Arch Gynecol Obstet

Author:

Zhang Mengting,Gao Yue,Liang Mingyu,Wang Yaoping,Guo Liangjie,Wu Dong,Xiao Hai,Lin Li,Wang Hongdan,Liao Shixiu

Funder

Henan Provincial Science and Technology Research Project

Henan Provincial Medical Science and Technology Research Project

Opening Foundation of National Health Commission Key Laboratory of Birth Defects Prevention

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s00404-024-07514-1.pdf

Reference27 articles.

1. Bull MJ (2020) Down syndrome. N Engl J Med 382(24):2344–2352. https://doi.org/10.1056/NEJMra1706537. (PMID: 32521135)

2. Wilmot HC, de Graaf G, van Casteren P, Buckley F, Skotko BG (2023) Down syndrome screening and diagnosis practices in Europe, United States, Australia, and New Zealand from 1990–2021. Eur J Hum Genet 31(5):497–503. https://doi.org/10.1038/s41431-023-01330-y. (Epub 2023 Mar 16 PMID: 36922634; PMCID: PMC10172164)

3. American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins-Obstetrics, Committee on Genetics, Society for Maternal-Fetal Medicine (2020) Screening for fetal chromosomal abnormalities: ACOG practice bulletin, number 226. Obstet Gynecol 136(4):e48–e69. https://doi.org/10.1097/AOG.0000000000004084. (PMID: 32804883)

4. Kagan KO, Sonek J, Kozlowski P (2022) Antenatal screening for chromosomal abnormalities. Arch Gynecol Obstet 305(4):825–835. https://doi.org/10.1007/s00404-022-06477-5. (Epub 2022 Mar 13 PMID: 35279726; PMCID: PMC8967741)

5. Benn P, Borrell A, Cuckle H, Dugoff L, Gross S, Johnson JA, Maymon R, Odibo A, Schielen P, Spencer K, Wright D, Yaron Y (2012) Prenatal detection of down syndrome using massively parallel sequencing (MPS): a rapid response statement from a committee on behalf of the board of the international society for prenatal diagnosis, 24 October 2011. Prenat Diagn 32(1):1–2. https://doi.org/10.1002/pd.2919. (Epub 2012 Jan 24 PMID: 22275335)

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