(Q66927325)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:480027%20AND%20SRC:MED&resulttype=core&format=json

31 August 2019

title

Holt-Oram syndrome (English)

1 reference

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31 August 2019

author name string

A T Smith

series ordinal

1

1 reference

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31 August 2019

G H Sack

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:480027%20AND%20SRC:MED&resulttype=core&format=json

31 August 2019

G J Taylor

series ordinal

3

1 reference

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31 August 2019

language of work or name

English

0 references

publication date

1 October 1979

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:480027%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

31 August 2019

published in

1 reference

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31 August 2019

volume

95

1 reference

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31 August 2019

issue

4

1 reference

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31 August 2019

page(s)

538-543

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:480027%20AND%20SRC:MED&resulttype=core&format=json

Familial heart disease with skeletal malformations

31 August 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Ultrasound scan in diagnosis of peripheral aneurysms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

FAMILIAL CONGENITAL MALFORMATIONS OF THE HEART AND UPPER LIMBS. A SYNDROME OF HOLT-ORAM

7 January 2021

1 reference

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7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

The syndrome of familial defects of heart and upper extremities (Holt-Oram syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

The syndrome of familial atrial septal defect, heart arrhythmia and hand malformation (Holt-Oram) in mother and son

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Anomalies associated with radial dysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Prolapsed Mitral Valve Associated with the Holt-Oram Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Holt-Oram syndrome associated with combined ostium primum and secundum atrial septal defects: Successful surgical closure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Atrial Septal Defect Associated with Skeletal Anomalies (Holt-Oram Syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Association of Holt-Oram syndrome and lymphosarcoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

A large deletion of the long arm of chromosome No. 4 in a child with limb abnormalities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Extending the scope of the VATER association: definition of the VATER syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Skeletal manifestations of the Holt-Oram syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Abnormal thumbs and physical diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

The influence of the nerve in regeneration of the amphibian extremity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Trophic function of neurons in transplanted neonatal ganglia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Neural crest defects. A neuroanatomic basis for classification of multiple malformations related to phocomelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

Congenital diaphragmatic hernia associated with homolateral upper limb malformation: A study of possible pathogenesis in four cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980758-1

10.1016/S0022-3476(79)80758-1

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:480027%20AND%20SRC:MED&resulttype=core&format=json

31 August 2019

1 reference