(Q36917507)

17 August 2017

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title

Genetics and congenital heart disease (English)

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17 August 2017

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congenital heart disease

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Emanuel R

1

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17 August 2017

1 May 1970

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17 August 2017

British Heart Journal

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17 August 2017

32

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17 August 2017

3

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17 August 2017

281-291

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Familial heart disease with skeletal malformations

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

FAMILIAL SUPRAVALVAR AORTIC STENOSIS

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

GENETIC ASPECTS OF CARDIOVASCULAR DISEASES IN ANIMALS.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Obstructive cardiomyopathy simulating aortic stenosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Congenital cardiac malformations in mongolism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Asymmetrical hypertrophy of the heart in young adults

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Discordant heart anomalies in twins.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Genetic and non-genetic factors in the etiology of congenital heart disease: a study of 1188 cases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

The patent ductus; a review of seventy-five cases with surgical treatment including an aneurysm of the ductus and one of the pulmonary artery

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Chromosome studies in 156 patients with congenital heart disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Incidence of congenital abnormalities in Liverpool, 1960-64

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Congenital Malformations in Autosomal Trisomy Syndromes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Atrial septal defect in three generations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Familial patent ductus arteriosus

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Gargoylism; a mucopolysaccharidosis.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

SOME FACTORS IN THE ETIOLOGY OF VENTRICULAR SEPTAL DEFECT.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

A GENETICAL VIEW OF CARDIOVASCULAR DISEASE. THE LEWIS A. CONNER MEMORIAL LECTURE.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

A family study of Fallot's tetrad

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=487321

Congenital malformations of the cardiovascular system in a series of 6,053 infants

20 October 2018

1 reference

12 December 2020

Congenital heart disease in the dog

1 reference

12 December 2020

TRISOMY 17-18(E): STUDIES IN LONG-TERM SURVIVAL WITH REPORT OF TWO AUTOPSIED CASES

1 reference

12 December 2020

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

1 reference

12 December 2020

Cardiac maliformation in mongolism

1 reference

12 December 2020

Hereditary factors in atrial septal defect

1 reference

12 December 2020

Ventricular septal defects in the fowl

1 reference

12 December 2020

Idiopathic hypertrophic subaortic stenosis. Clinical analysis of 126 patients with emphasis on the natural history

1 reference

12 December 2020

A survey of congenital heart disease in a children's hospital, with special reference to surgical treatment

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial congenital heart disease. II. Chromosomal studies

1 reference

12 December 2020

Congenital Heart Disease in Twins

1 reference

12 December 2020

Congenital Cardiovascular Anomalies in Twins

1 reference

12 December 2020

Genetic Transmission of Congenital Membranous Ventricular Septal Defects in Selectively Inbred Substrains of Rats

1 reference

12 December 2020

Thalidomide disaster considered as an experiment in mammalian teratology

1 reference

12 December 2020

1 reference

12 December 2020

The heart in Turner-Ullrich syndrome. (Study of 26 personal cases and review of cases comprising a chromosomal study)

1 reference

12 December 2020

Upper-limb cardiovascular syndrome. A family study

1 reference

12 December 2020

Twins and congenital heart disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary transmission of patent ductus arteriosus in the dog

1 reference

12 December 2020

Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/HRT.32.3.281

1 reference

17 August 2017

1 reference

PMC publication ID

487321

17 August 2017

PubMed publication ID

4246190

1 reference

PMC publication ID

487321