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Article

Genetic background of congenital conotruncal heart defects--a study of 45 families.

Kardiologia polska - 1 Jan 2007

Kwiatkowska Joanna, Wierzba Jolanta, Aleszewicz-Baranowska Janina, Ereciński Jan

Abstract excerpt

INTRODUCTION: The latest achievements in molecular diagnosis create new possibilities for evaluation of congenital abnormalities. AIM: To present our preliminary experience with genetic diagnosis of congenital combined conotruncal heart defects. METHODS: The analysis comprised 35 families with more than one member suffering from conotruncal heart defects (Group I) and 10 families (Group II) having a child with...

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Share to Abnormalities, Multiple
Share to Causality
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 22

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Share to Heart Defects, Congenital

Share to In Situ Hybridization, Fluorescence

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PMID: 17295158

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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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