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Article

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency

24 May 2017

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28540525
DOI: 10.1007/s10875-017-0403-9

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined ImmunodeficiencyPMID 28540525Read ↗

Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screeningSemantic proximity Read ↗

Immunodeficiency in a Child with 22q11.2 Microduplication Syndrome.Semantic proximity Read ↗

Our evolving understanding of 22q.11 deletion syndrome.Semantic proximity Read ↗

Development of population-based newborn screening for severe combined immunodeficiencySemantic proximity Read ↗

The 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive valueSemantic proximity Read ↗

Deletion 22q11: Spectrum of Associated DisordersSemantic proximity Read ↗

Newborn screening programs: should 22q11 deletion syndrome be added?Semantic proximity Read ↗

22q11.2 deletion syndromeSemantic proximity Read ↗

Unraveling the genetic and developmental mysteries of 22q11 deletion syndromeSemantic proximity Read ↗

Development of a routine newborn screening protocol for severe combined immunodeficiencySemantic proximity Read ↗

Chromosome 22q11.2 deletion syndrome.Semantic proximity Read ↗

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