(Q55843613)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Congenital heart disease, deafness, and skeletal malformations: a new syndrome? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

Congenital heart disease, deafness, andskeletal malformations: A new syndrome? (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

11 July 2023

main subject

congenital heart disease

1 reference

1 reference

W. R. Forney

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901343

11 July 2023

S. J. Robinson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901343

11 July 2023

D. J. Pascoe

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5901343

11 July 2023

language of work or name

English

0 references

publication date

1 January 1966

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

29 October 2019

https://api.elsevier.com/content/article/PII:S0022347666804183?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

https://api.elsevier.com/content/article/PII:S0022347666804183?httpAccept=text/plain

11 July 2023

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

The Journal of Pediatrics

11 July 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

68

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

page(s)

14-26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

A Syndrome Characterized by Ectodermal Dysplasia, Polydactyly, Chondro-Dysplasia and Congenital Morbus Cordis: Report of Three Cases

29 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Single atrium and the Ellis-van Creveld syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Cardiac anomalies in mongolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Cardiac malformation in mongolism: a prospective study of 184 mongoloid children

7 January 2021

1 reference

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Cardiovascular lesions in arachnodactyly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

The cardiovascular aspects of Marfan's syndrome: a heritable disorder of connective tissue

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Congenital mesodermal dysmorpho-dystrophy (brachymorphic type)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Familial heart disease with skeletal malformations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

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%2866%2980418-3

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%2866%2980418-3

An aetiological study of congenital heart disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Familial occurrence of congenital heart disease: report of three families and review of the literature

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

A report of congenital heart disease in five members of one family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

ISOLATED CONGENITAL MITRAL INSUFFICIENCY

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Multiple anomalies in gongenitally deaf children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Congenital deafness associated with onychodystrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Clinical experiences in tympanoplasty; results in sixty-one cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Symphalangism, strabismus and hearing loss in mother and daughter.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Familial nephrosis associated with deafness and congenital urinary tract anomalies in siblings.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Deafness as part of an hereditary syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Congenital deaf-mutism, prolonged QT interval, syncopal attacks and sudden death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

The use of dermal configurations in the diagnosis of mongolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

The distal triradius t on the hands of parents and sibs of mongol imbeciles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Finger-Prints, Palms and Chromosomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

FINGERPRINTS AND PALM PRINTS (DERMATOGLYPHICS) AND PALMAR-FLEXION CREASES IN GONADAL DYSGENESIS, PSEUDOHYPOPARATHYROIDISM AND KLINEFELTER'S SYNDROME

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Features of palmar dermatoglyphics in congenital heart disease. A report on the variants frequently associated with congenital lesions of the heart

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

The third interdigital patterns on the palms of the general British population, mongoloid and non-mongoloid mental defectives.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

HEART DISEASE IN THE LAURENCE-MOON-BIEDL-BARDET SYNDROME: A REVIEW AND A REPORT OF 3 BROTHERS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

Deafness and the Laurence-Moon-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

PROFOUND CHILDHOOD DEAFNESS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2866%2980418-3

inferred from DOI database lookup

7 January 2021

based on heuristic

The heart in arachnodactyly

7

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

Skeletal abnormalities associated with gonadal dysgenesis

11 July 2023

10

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

Congenital talonavicular synostosis associated with hereditary multiple ankylosing arthropathies

11 July 2023

26

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

Symphalangism and related fusions of tarsal bones

11 July 2023

27

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(66)80418-3

11 July 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5901343%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference