Holt-Oram syndrome: a clinical genetic study (Q33677213)

28 July 2017

title

Holt-Oram syndrome: a clinical genetic study (English)

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28 July 2017

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Newbury-Ecob RA

1

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28 July 2017

Leanage R

series ordinal

2

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28 July 2017

Raeburn JA

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3

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28 July 2017

Young ID

series ordinal

4

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28 July 2017

language of work or name

English

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publication date

1 April 1996

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

33

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28 July 2017

issue

4

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28 July 2017

page(s)

300-307

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Familial heart disease with skeletal malformations

28 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

Spectrum of anomalies in Fanconi anaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

A population study of the VACTERL association: evidence for its etiologic heterogeneity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

Holt-Oram syndrome: clinical and genetic study of a large family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

The upper limb-cardiovascular syndrome. A report of two African cases with a review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

The "long-thumb" brachydactyly syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050579

The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis

30 October 2018

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12 December 2020

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12 December 2020

A girl with severe expression of the Holt-Oram gene

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12 December 2020

Variable expression of the Holt-Oram syndrome

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12 December 2020

Anomalies associated with radial dysplasia

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12 December 2020

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12 December 2020

Thrombocytopenia and absent radius (TAR) syndrome

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12 December 2020

Prenatal ultrasound diagnosis of the Holt-Oram syndrome

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12 December 2020

Heart-hand syndrome II. A report of Tabatznik syndrome with new findings

1 reference

12 December 2020

Familial atrial septal defect with prolonged atrioventricular conduction

1 reference

12 December 2020

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

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12 December 2020

Retreat of the triplet repeat?

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12 December 2020

CONGENITAL HEART DISEASE AND UPPER-EXTREMITY DEFORMITIES: A REPORT OF TWO FAMILIES

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12 December 2020

Heart-hand syndrome. III. A new syndrome in three generations

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12 December 2020

Holt Oram syndrome mistaken for thalidomide embryopathy--embryological considerations

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12 December 2020

Holt-Oram syndrome: penetrance of the gene and lack of maternal effect

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.33.4.300

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28 July 2017

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28 July 2017

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