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Article

Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.

Molecular medicine reports - 1 Feb 2018

Zhang Lin, Ren Meihong, Song Guining, Zhang Yang, Liu Xuexia, Zhang Xiaohong, Wang Jianliu

Abstract excerpt

The aim of the present study was to perform comprehensive prenatal diagnosis using various detection techniques on a fetus in a high‑risk pregnant woman, and to provide genetic counseling for the patient and her family so as to avoid birth defects. The routine karyotype analysis via amniocentesis, fluorescence in situ hybridization, and whole genome microarray technique were performed for the prenatal diagnosis...

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Share to Amniocentesis
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Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 29257243
DOI: 10.3892/mmr.2017.8198
PMCID: PMC5783495

Genes

SRY
STS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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