Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome

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Main Authors: Mani Ram Krishna, Usha Nandhini Sennaiyan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-01-01
Series:Annals of Pediatric Cardiology
Online Access:https://journals.lww.com/10.4103/apc.apc_45_25
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author Mani Ram Krishna
Usha Nandhini Sennaiyan
author_facet Mani Ram Krishna
Usha Nandhini Sennaiyan
author_sort Mani Ram Krishna
collection DOAJ
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issn 0974-2069
0974-5149
language English
publishDate 2025-01-01
publisher Wolters Kluwer Medknow Publications
record_format Article
series Annals of Pediatric Cardiology
spelling doaj-art-fe510dacede34689b1f772811c47e0862025-08-20T02:56:32ZengWolters Kluwer Medknow PublicationsAnnals of Pediatric Cardiology0974-20690974-51492025-01-01181858610.4103/apc.apc_45_25Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndromeMani Ram KrishnaUsha Nandhini Sennaiyanhttps://journals.lww.com/10.4103/apc.apc_45_25
spellingShingle Mani Ram Krishna
Usha Nandhini Sennaiyan
Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
Annals of Pediatric Cardiology
title Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
title_full Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
title_fullStr Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
title_full_unstemmed Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
title_short Isolated aortic root dilatation – Expanding the cardiac phenotype of 22q11 deletion syndrome
title_sort isolated aortic root dilatation expanding the cardiac phenotype of 22q11 deletion syndrome
url https://journals.lww.com/10.4103/apc.apc_45_25
work_keys_str_mv AT maniramkrishna isolatedaorticrootdilatationexpandingthecardiacphenotypeof22q11deletionsyndrome
AT ushanandhinisennaiyan isolatedaorticrootdilatationexpandingthecardiacphenotypeof22q11deletionsyndrome