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March 10, 2024

[Prenatal ultrasonographic manifestations and genetic diagnosis of nine fetuses with 7q11.23 duplication syndrome].

Pengyun Li Jing Guo Jia Che Fangying Cui Yuexia Lyu Hua Zhang Ying Li Ling Liu

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Abstract

To analyze ultrasonographic manifestations and genetic etiology of nine fetuses with 7q11.23 duplication syndrome.

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Cite This Study

Li et al. (2024) studied this question.

synapsesocial.com/papers/68e74cd0b6db6435876c5430 https://doi.org/10.3760/cma.j.cn511374-20221117-00795

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

1Characterization of the Prenatal Ultrasound Phenotype Associated With 7q11.23 Microduplication Syndrome and Williams–Beuren Syndrome2024
2Prenatal Diagnosis, Ultrasound Findings, and Follow-up Information of 1q21.1 Deletion and Duplication Syndromes: A Single-Center Case Series2025
3[Clinical and genetic analysis of ten Chinese pedigrees affected with 7q11.23 duplication syndrome].2024
4Case Report: Prenatal diagnosis of 10 fetuses with 15q11-q13 duplication and pregnancy outcome in a cohort of Chinese women2025 · 1 citations
5Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound AnomaliesOriginal Research · 2018 · 13 citations

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