Deletion 22q11 in patients with interrupted aortic arch (Q58193949)

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31 October 2019

title

Deletion 22q11 in patients with interrupted aortic arch (English)

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31 October 2019

main subject

interrupted aortic arch

1 reference

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31 October 2019

B Marino

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31 October 2019

M C Digilio

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31 October 2019

M Persiani

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31 October 2019

R Di Donato

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31 October 2019

A Toscano

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31 October 2019

A Giannotti

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31 October 2019

language of work or name

English

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publication date

1 August 1999

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American Journal of Cardiology

31 October 2019

published in

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31 October 2019

volume

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31 October 2019

issue

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31 October 2019

page(s)

360-1, A9

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Interruption of the aortic arch and coarctation of the aorta: pathogenetic relations.

31 October 2019

cites work

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Interrupted right aortic arch in DiGeorge syndrome

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Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome

7 January 2021

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

7 January 2021

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Congenital absence of the aortic arch

7 January 2021

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A Genetic Etiology for Interruption of the Aortic Arch Type B

7 January 2021

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Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch

7 January 2021

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Frequency of 22q11 deletions in patients with conotruncal defects

7 January 2021

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Association of interrupted aortic arch with malformations producing reduced blood flow to the fourth aortic arches

7 January 2021

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Ventricular septal defect in interruption of aortic arch

7 January 2021

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Interruption of the aortic arch with aorticopulmonary septal defect. An anatomic review

7 January 2021

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Operative mortality and frequency of coexistent anomalies in interruption of the aortic arch

7 January 2021

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Complete transposition of great arteries with coarctation of aorta

7 January 2021

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Anatomy and pathogenesis of aorticopulmonary septal defect.

7 January 2021

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Associated cardiac anomalies in isolated and syndromic patients with tetralogy of Fallot.

7 January 2021

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Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome

7 January 2021

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22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

7 January 2021

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Cardiac malformations in relatives of children with truncus arteriosus or interruption of the aortic arch

7 January 2021

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UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

7 January 2021

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A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

7 January 2021

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10.1016/S0002-9149(99)00297-0

7 January 2021

Identifiers

DOI

1 reference

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31 October 2019

1 reference

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