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February 10, 2024

[Genetic diagnosis and analysis of eight cases with central 22q11.2 deletion syndrome].

Jing Guo Pengyun Li Jia Che Shanshan Zhai Weifang Tian Ying Li Hua Zhang Ling Liu

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Abstract

To explore the pregnancy outcome and postpartum clinical phenotype of LCR22B/C~D central 22q11.2 deletion syndrome.

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Cite This Study

Guo et al. (2024) studied this question.

synapsesocial.com/papers/68e79c4cb6db64358770b699 https://doi.org/10.3760/cma.j.cn511374-20221125-00812

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Expanding the Prenatal Phenotype and Genotype of 22q11.2 Deletion Syndrome through Genome-wide Chromosomal Microarray AnalysisReview · 2026
2Clinical Course and Outcome of Prenatally Detected 22q11.2 Deletion Syndrome—A Retrospective AnalysisCohort Study · 2023 · 4 citations
3Correlation between 22q11.2 deletion syndrome phenotype and deletion location: a meta-analysisMeta-Analysis · 2025 · 4 citations
4Prenatal Diagnosis and Clinical Phenotypic Heterogeneity of 22q11.2 Microdeletion Syndrome Based on a Single Center Retrospective StudyRetrospective Study · 2025
5Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome.Original Research · 2026 · 1 citations

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Genetic Mapping of the 22q11.2 Deletion Syndrome (DiGeorge Syndrome) Microdeletion Types Revealed Novel Candidate Breakpoints2026