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Article

Characterization of 10p Deletions Suggests Two Nonoverlapping Regions Contribute to the DiGeorge Syndrome Phenotype

1 Feb 1998

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Identifiers

PMID: 9463325
DOI: 10.1086/301718

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of 10p Deletions Suggests Two Nonoverlapping Regions Contribute to the DiGeorge Syndrome PhenotypePMID 9463325Read ↗

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)Semantic proximity Read ↗

A Novel 22q11.2 Microdeletion in DiGeorge SyndromeSemantic proximity Read ↗

DiGeorge Syndrome: New InsightsSemantic proximity Read ↗

Genetic dissection of the DiGeorge syndrome phenotype.Semantic proximity Read ↗

The Diverse Clinical Features of Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome)Semantic proximity Read ↗

DiGeorge syndrome: an historical review of clinical and cytogenetic features.Semantic proximity Read ↗

DiGeorge's syndrome: a gene at last.Semantic proximity Read ↗

The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniquesSemantic proximity Read ↗

Genetics: Genetic and functional studies reveal genetic drivers of renal disease in DiGeorge syndrome.Semantic proximity Read ↗

The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.Semantic proximity Read ↗

22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial SyndromeSemantic proximity Read ↗

DiGeorge anomaly associated with 10p deletionSemantic proximity Read ↗

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