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Article

[Prenatal diagnosis of 17q12 microdeletion syndrome in fetal renal abnormalities].

Zhonghua fu chan ke za zhi - 25 Oct 2017

Jiang Y L, Qi Q W, Zhou X Y, Geng F F, Bai J J, Hao N, Liu J T

Abstract excerpt

Objectives: To analyze 3 cases of 17q12 microdeletion syndrome diagnosed prenatally, and to demonstrate clinical phenotype of the syndrome in prenatal setting. Methods: From January 2013 to July 2017, 1 370 women received invasive prenatal diagnosis and chromosome microarray analysis (CMA) in Peking Union Medical College Hospital. Among them, 3 fetuses were diagnosed as 17q12 microdeletion syndrome. All 3 cases...

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 17

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 29060963
DOI: 10.3760/cma.j.issn.0529-567X.2017.10.004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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