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Article

Newborn screening programs: should 22q11 deletion syndrome be added?

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Mar 2010

Bales Abigail M, Zaleski Christina A, McPherson Elizabeth W

Abstract excerpt

The highly variable 22q11 deletion syndrome has been proposed for addition to newborn screening panels. A literature review investigated the incidence and prevalence, clinical features, and prognosis of 22q11 deletion syndrome and other issues related to newborn screening. Severe complications th...

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 22

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

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Source

Identifiers

PMID: 20071995
DOI: 10.1097/GIM.0b013e3181cdeb9a

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20071995-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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