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Article

Anatomic patterns of conotruncal defects associated with deletion 22q11.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Jan 2000

Marino B, Digilio M C, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris M A, Angioni A, Dallapiccola B

Abstract excerpt

PURPOSE: Patients with cardiovascular malformations (CVMs) and deletion 22q11 from our series were studied in order to (1) analyze the association with dysmorphic features and noncardiac anomalies, (2) identify specific cardiac patterns and the distinctive association with additional CVMs. METHODS: From 1993 to 2000, 931 patients with CVM (95 with a clinical diagnosis of DiGeorge/velocardiofacial syndrome...

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Share to Abnormalities, Multiple
Share to Aorta, Thoracic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Deletion

Share to Chromosomes, Human, Pair 22

Share to DiGeorge Syndrome

Share to Heart Defects, Congenital

Share to Heart Septal Defects, Ventricular

Share to Tetralogy of Fallot

Source

Identifiers

PMID: 11339377
DOI: 10.1097/00125817-200101000-00010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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