A Genetic Etiology for Interruption of the Aortic Arch Type B (Q73670410)

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5 November 2019

title

A genetic etiology for interruption of the aortic arch type B (English)

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5 November 2019

A Genetic Etiology for Interruption of the Aortic Arch Type B (English)

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chromosomal deletion syndrome

14 November 2024

main subject

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A. Baldini

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M. B. Lewin

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E. A. Lindsay

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V. Jurecic

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V. Goytia

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J. A. Towbin

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language of work or name

English

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publication date

1 August 1997

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5 November 2019

15 August 1997

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National Center for Biotechnology Information

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full work available at URL

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American Journal of Cardiology

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published in

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volume

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issue

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page(s)

493-497

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Role of neural crest in congenital heart disease

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Alteration of early vascular development after ablation of cranial neural crest

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

DiGeorge syndrome and 22q11 rearrangements

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Neural crest cells contribute to normal aorticopulmonary septation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Cardiac neural crest is essential for the persistence rather than the formation of an arch artery

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Deletion within chromosome 22 is common in patients with absent pulmonary valve syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

Fetal alcohol syndrome and DiGeorge anomaly: critical ethanol exposure periods for craniofacial malformations as illustrated in an animal model

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2897%2900401-3

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7 January 2021

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Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome

1 reference

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Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies

14 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0002-9149(97)00401-3

Isotretinoin teratogenicity in mouse whole embryo culture

14 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0002-9149(97)00401-3

14 November 2024

Identifiers

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5 November 2019

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