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Article

Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: A prospective study

1 Nov 1995

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8582397
DOI: 10.1007/bf01957496

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Related research

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Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: A prospective studyPMID 8582397Read ↗

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[Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].Semantic proximity Read ↗

Anatomic patterns of conotruncal defects associated with deletion 22q11.Semantic proximity Read ↗

Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects.Semantic proximity Read ↗

22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype.Semantic proximity Read ↗

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