Prenatal Diagnosis of Microdeletions or Microduplications in the Proximal, Central, and Distal Regions of Chromosome 22q11.2: Ultrasound Findings and Pregnancy Outcome-Reference-Cited by-同舟云学术

Prenatal Diagnosis of Microdeletions or Microduplications in the Proximal, Central, and Distal Regions of Chromosome 22q11.2: Ultrasound Findings and Pregnancy Outcome

Published:2019-08-30 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Li Shuyuan,Han Xu,Ye Mujin,Chen Songchang,Shen Yinghua,Niu Jianmei,Wang Yanlin,Xu Chenming

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

National Basic Research Program of China (973 Program)

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference36 articles.

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4. Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1;Breckpot;Am. J. Med. Genet. A,2012

5. 22q11.21 Deletion syndromes: a review of proximalcentral, and distal deletions and their associated features;Burnside;Cytogenet. Genome Res.,2015

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1. Prenatal diagnosis and genetic study of 22q11.2 microduplication in Chinese fetuses: A series of 31 cases and literature review;Molecular Genetics & Genomic Medicine;2024-07

2. Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array;Journal of Personalized Medicine;2024-03-08

3. Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment in Danish nationwide cohort;Ultrasound in Obstetrics & Gynecology;2024-01

4. Pathogenic recurrent copy number variants in 7,078 pregnancies via chromosomal microarray analysis;Journal of Perinatal Medicine;2023-12-12

5. The Subtlety of 22q11.2 Deletion Syndrome in a Preterm Neonate;Neonatal Network;2023-05-01