(Q52177233)

26 April 2018

title

Associations between chromosomal anomalies and congenital heart defects: a database search. (English)

1 reference

26 April 2018

author name string

van Karnebeek CD

series ordinal

1

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26 April 2018

Hennekam RC

series ordinal

2

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26 April 2018

publication date

1 May 1999

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26 April 2018

American Journal of Medical Genetics Part A

published in

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26 April 2018

volume

84

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26 April 2018

issue

2

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26 April 2018

page(s)

158-166

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26 April 2018

Mouse GATA-4: a retinoic acid-inducible GATA-binding transcription factor expressed in endodermally derived tissues and heart

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Familial risks of congenital heart defect assessed in a population-based epidemiologic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Deficiency of chromosome 8p21.1----8pter: case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Incidence of congenital heart disease: I. Postnatal incidence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Toward a molecular understanding of congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

The use of multiple thresholds in determining the mode of transmission of semi-continuous traits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Variation in severity of cardiac disease in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Assignment of the human GATA4 gene to 8p23.1-->p22 using fluorescence in situ hybridization analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Deletions within chromosome 22q11 in familial congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

Abnormal laterality and congenital cardiac anomalies. Relations of visceral and cardiac morphologies in the iv/iv mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990521%2984%3A2%3C158%3A%3AAID-AJMG13%3E3.0.CO%3B2-5

10.1002/(SICI)1096-8628(19990521)84:2<158::AID-AJMG13>3.0.CO;2-5

21 January 2018

Identifiers

DOI

1 reference

26 April 2018

PubMed ID

10323742

1 reference

26 April 2018