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Comment
. 2021 Jan;23(1):234-235.
doi: 10.1038/s41436-020-00964-3. Epub 2020 Sep 27.

Correspondence on "The prevalence of genetic diagnoses in fetuses with severe congenital heart defects" by Nisselrooij et al

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Comment

Correspondence on "The prevalence of genetic diagnoses in fetuses with severe congenital heart defects" by Nisselrooij et al

My Linh Thibodeau et al. Genet Med. 2021 Jan.
Free article
No abstract available

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  • Response to Thibodeau and Langlois.
    van Nisselrooij AEL, Aten E, Santen GWE, Haak MC. van Nisselrooij AEL, et al. 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.

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References

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    1. 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
    1. 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
    1. 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
    1. 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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