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Foetal phenotype of ALG1-CDG caused by paternal uniparental disomy 16.

作者信息

Lei Ya-Li, Zhen Li, Xu Li-Li, Yang Yan-Dong, Li Dong-Zhi

机构信息

Clinical Laboratory, Dongguan Kanghua Hospital, Dongguan, China.

Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou, China.

出版信息

J Obstet Gynaecol. 2021 Jul;41(5):828-830. doi: 10.1080/01443615.2020.1786031. Epub 2020 Aug 19.

DOI:10.1080/01443615.2020.1786031
PMID:32811240
Abstract
摘要

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引用本文的文献

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Front Genet. 2022 Dec 13;13:1019283. doi: 10.3389/fgene.2022.1019283. eCollection 2022.
2
ALG1-CDG: A Patient with a Mild Phenotype and Literature Review.ALG1-先天性糖基化障碍:一名具有轻度表型的患者及文献综述
Mol Syndromol. 2022 Feb;13(1):69-74. doi: 10.1159/000517797. Epub 2021 Sep 21.
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ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.
由涉及新型致病复合等位基因的无功能可变剪接引起的ALG1-CDG
Front Genet. 2021 Sep 9;12:744884. doi: 10.3389/fgene.2021.744884. eCollection 2021.