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Article

Prenatal detection of rare chromosomal autosomal abnormalities in Europe

7 Feb 2003

Abstract excerpt

The aim of the present study was to evaluate the prenatal detection of rare chromosomal autosomal abnormalities by ultrasound (US) examination. Data were obtained from 19 congenital malformation registries from 11 European countries, between 01/07/96 and 31/12/98. A total of 664,340 births were covered and 7,758 cases with congenital malformations were recorded. Rare autosomal abnormalities were diagnosed in 114...

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Share to Congenital Anomalies and Fetal Surgery
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Identifiers

PMID: 12687662
DOI: 10.1002/ajmg.a.10104

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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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