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Article

[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 10 Dec 2017

Ji Xiuqing, Hu Huanran, Wang Yan, Liang Dong, Luo Chunyu, Meng Lulu, Zhou Jing, Cao Li, Ma Dingyuan, Hu Ping, Xu Zhengfeng

Abstract excerpt

OBJECTIVE: To analyze two fetuses with multiple malformations revealed by ultrasonography using single nucleotide polymorphism array (SNP array), and to explore the strategy for the prenatal diagnosis of 1p36 deletion syndrome. METHODS: Amniocentesis was performed on the two pregnant women. Amnion fluid cells were cultured, and karyotypes of the fetuses were determined through G-banding analysis. Whole genome SNP...

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Identifiers

PMID: 29188615
DOI: 10.3760/cma.j.issn.1003-9406.2017.06.015

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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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