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Article

[Prenatal diagnosis of two fetuses with de novo 46,X,psu dic(Y)/45,X mosaicism].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Sept 2020

Chen Jiayan, Chen Xiaolu, Cai Meijiao, Zhang Jian, Ge Yunsheng

Abstract excerpt

OBJECTIVE: To carry out prenatal diagnosis for a fetus with increased nuchal translucency (NT) and another fetus with non-invasive prenatal testing (NIPT) suggested reduced sex chromosomes by cytogenetic and molecular techniques. METHODS: Chromosomal karyotyping, single nucleotide polymorphism array (SNP-array) and fluorescence in situ hybridization (FISH) were applied for the diagnoses. Peripheral blood samples...

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Share to Chromosomes, Human, Y
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

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Share to Polymorphism, Single Nucleotide

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Identifiers

PMID: 32820525
DOI: 10.3760/cma.j.cn511374-20191015-00527

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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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