(Q41415560)

30 September 2017

1 reference

title

The genetic basis of pediatric cardiovascular disease (English)

1 reference

30 September 2017

Strauss AW

1

1 reference

PubMed ID

9090781

30 September 2017

Johnson MC

series ordinal

2

1 reference

30 September 2017

1 December 1996

1 reference

30 September 2017

Seminars in Perinatology

1 reference

30 September 2017

20

1 reference

30 September 2017

6

1 reference

30 September 2017

564-576

1 reference

Report of the task force on children and youth. American Heart Association

30 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Molecular pathways controlling heart development

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Toward a molecular understanding of congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

A mouse model of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Familial hypertrophic cardiomyopathy. Nonsense versus missense mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Fatty acid oxidation disorders: A new class of metabolic diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Lethal neonatal multiorgan deficiency of carnitine palmitoyltransferase II

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Clinical approach to genetic cardiomyopathy in children

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mouse mutants and cardiac development: new molecular insights into cardiogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Incidence of congenital heart disease: I. Postnatal incidence.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Transcriptional enhancer factor 1 disruption by a retroviral gene trap leads to heart defects and embryonic lethality in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

RXR alpha deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Identification of an essential nonneuronal function of neurotrophin 3 in mammalian cardiac development

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Cardiac malformation in neonatal mice lacking connexin43.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

NK-2 homeobox genes and heart development

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

A subclass of bHLH proteins required for cardiac morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

DiGeorge syndrome: part of CATCH 22.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Chromosome 22q11 monosomy and the genetic basis of congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Discrete membranous subaortic stenosis in siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Familial occurrence of discrete subaortic membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Familial atrioventricular septal defect: possible genetic mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Familial heart disease with skeletal malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Genetic heterogeneity of heart-hand syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Cardiologic abnormalities in Noonan syndrome: phenotypic diagnosis and echocardiographic assessment of 118 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Father and two children with total anomalous pulmonary venous connection

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Tricuspid atresia and annular hypoplasia: report of a familial occurrence

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Familial Ebstein's anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Congenital malformations of the tricuspid valve in siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

Genetic study of congenital heart defects in Northern Ireland (1974-1978)

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2896%2980069-3

7 January 2021

10.1016/S0146-0005(96)80069-3

Identifiers

DOI

1 reference

30 September 2017

1 reference

PubMed ID

9090781