Special Situations in Aneuploidy Screening
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-99-7758-1_11
Reference20 articles.
1. Gair JL, Arbour L, Rupps R, Jiang R, Bruyère H, Robinson WP. Recurrent trisomy 21: four cases in three generations. Clin Genet. 2005;68(5):430–5.
2. Kolgeci S, Kolgeci J, Azemi M, Shala-Beqiraj R, Gashi Z, Sopjani M. Cytogenetic study in children with down syndrome among kosova Albanian population between 2000 and 2010. Mater Sociomed. 2013;25(2):131–5.
3. Kovaleva NV. Germ-line transmission of trisomy 21: data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue. Mol Cytogenet. 2010;3:7.
4. Wu X, He S, Li Y, Guo D, Chen X, Liang B, Wang M, Huang H, Xu L. Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience. BMC Pregnancy Childbirth. 2023;23(1):73.
5. Meler E, Sisterna S, Borrell A. Genetic syndromes associated with isolated fetal growth restriction. Prenat Diagn. 2020;40(4):432–46.
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