An Incidental Detection of a Rare UPD in SNP-Array Based PGT-SR: A Case Report-Reference-Cited by-同舟云学术

An Incidental Detection of a Rare UPD in SNP-Array Based PGT-SR: A Case Report

Published:2024-05-23 Issue:9 Volume:31 Page:2893-2899
ISSN:1933-7191
Container-title:Reproductive Sciences
language:en
Short-container-title:Reprod. Sci.

Author:

Ma Yuanlin,wang Jing,Wen Tianrui,Xu Yan,Huang Linhuan,Mai Qingyun,Xu Yanwen^ORCID

Funder

National Key Research and Development Program of China

Guangzhou Science and Technology Project

Jieping Wu Medical Foundation Clinical Medical Research Project

Key Clinical Technique of Guangzhou, Guangdong Province, China

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s43032-024-01598-5.pdf

Reference17 articles.

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4. Xu J, Zhang Z, Niu W et al. Mapping allele with resolved carrier status of Robertsonian and reciprocal translocation in human preimplantation embryos. Proceedings of the National Academy of Sciences. 2017;114(41):E8695-E8702. https://doi.org/10.1073/pnas.1715053114.

5. Li R, Wang J, Gu A, et al. Feasibility study of using unbalanced embryos as a reference to distinguish euploid carrier from noncarrier embryos by single nucleotide polymorphism array for reciprocal translocations. Prenat Diagn. 2021;41(6):681–9. https://doi.org/10.1002/pd.5897.