(Q64864380)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096596%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder (English)

1 reference

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12 November 2019

author name string

A Mégarbané

1

1 reference

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12 November 2019

E Stephan

2

1 reference

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12 November 2019

R Kassab

3

1 reference

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12 November 2019

R Ashoush

4

1 reference

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12 November 2019

N Salem

5

1 reference

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12 November 2019

P Bouvagnet

6

1 reference

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12 November 2019

J Loiselet

7

1 reference

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12 November 2019

publication date

1 March 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096596%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

12 November 2019

published in

1 reference

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12 November 2019

volume

83

1 reference

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12 November 2019

issue

3

1 reference

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12 November 2019

page(s)

193-200

1 reference

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Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C193%3A%3AAID-AJMG10%3E3.0.CO%3B2-M

Familial atrial septal defect with prolonged atrioventricular conduction. A syndrome showing the autosomal dominant pattern of inheritance

21 January 2018

1 reference

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An isolated cardiac conduction disease maps to chromosome 19q

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C193%3A%3AAID-AJMG10%3E3.0.CO%3B2-M

Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C193%3A%3AAID-AJMG10%3E3.0.CO%3B2-M

Hereditary atrial septal defect. Update of a large kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C193%3A%3AAID-AJMG10%3E3.0.CO%3B2-M

Congenital heart disease caused by mutations in the transcription factor NKX2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990319%2983%3A3%3C193%3A%3AAID-AJMG10%3E3.0.CO%3B2-M

Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristics

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19990319)83:3<193::AID-AJMG10>3.0.CO;2-M

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10096596%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference