June 10, 2024

Genetic analysis of two families with abnormal findings upon prenatal diagnosis.

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Abstract

To carry out genetic analysis on two families with carriers of small terminal translocations using karyotyping analysis and genomic copy number variation sequencing (CNV-seq).

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Cite This Study

Wang et al. (Mon,) studied this question.

synapsesocial.com/papers/68e65761b6db6435875e5d50 https://doi.org/https://doi.org/10.3760/cma.j.cn511374-20220411-00242

Also Consider

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

1[Precise genetic analysis and reproductive guidance for two rare families with complex chromosomal rearrangements facilitated by optical genome mapping].2025
2Genome sequencing-based CNV analysis in an infant with concurrent partial trisomies 9p and 12p due to maternal translocation: A case report2026
3Karyotype Analysis and Chromosomal Microarray Analysis in 568 Couples with Balanced Translocation for Prenatal Diagnosis2026
4Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies2026
5Advancing Prenatal Diagnosis: From Conventional Karyotyping to Genome-Wide CNV Analysis2026 · 1 citations

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