Correspondence on "The prevalence of genetic diagnoses in fetuses with severe congenital heart defects" by Nisselrooij et al
- PMID: 32980861
- DOI: 10.1038/s41436-020-00964-3
Correspondence on "The prevalence of genetic diagnoses in fetuses with severe congenital heart defects" by Nisselrooij et al
Comment in
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Response to Thibodeau and Langlois.Genet Med. 2021 Jan;23(1):244-245. doi: 10.1038/s41436-020-00965-2. Epub 2020 Sep 27. Genet Med. 2021. PMID: 32980862 No abstract available.
Comment on
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The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.Genet Med. 2020 Jul;22(7):1206-1214. doi: 10.1038/s41436-020-0791-8. Epub 2020 Apr 28. Genet Med. 2020. PMID: 32341573 Free PMC article.
References
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- van Nisselrooij AEL, Lugthart MA, Clur S-A, et al. The prevalence of genetic diagnoses in fetuses with severe congenital heart defects. Genet Med. 2020;22:1206–1214. - DOI
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- Wang Y, Cao L, Liang D, et al. Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study. Am J Obstet Gynecol. 2018;218:244.e1–244.e17. - DOI
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- Song T, Wan S, Li Y, et al. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype. J Clin Lab Anal. 2019;33:e22630. - DOI
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- Lin M, Zheng J, Peng R, et al. Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array. J Matern Fetal Neonatal Med. 2020;33:1211–1217. - DOI
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- Morlando M, Bhide A, Familiari A, et al. The association between prenatal atrioventricular septal defects and chromosomal abnormalities. Eur J Obstet Gynecol Reprod Biol. 2017;208:31–35. - DOI
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