(Q36402060)

14 August 2017

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title

Congenital heart diseases in small animals: part II. Potential genetic aetiologies based on human genetic studies (English)

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14 August 2017

0 references

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Changbaig Hyun

1

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14 August 2017

In-Chul Park

series ordinal

2

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14 August 2017

publication date

1 March 2006

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14 August 2017

published in

The Veterinary Journal

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14 August 2017

volume

171

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14 August 2017

issue

2

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14 August 2017

page(s)

256-262

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

14 August 2017

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Canine tricuspid valve malformation, a model of human Ebstein anomaly, maps to dog chromosome 9.

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An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

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Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

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Congenital heart disease in adults. First of two parts

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Congenital heart disease in adults. Second of two parts

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Ebstein anomaly associated with rearrangements of chromosomal region 11q

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Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

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

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GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

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NKX2.5 mutations in patients with tetralogy of fallot

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inferred from DOI database lookup

7 January 2021

based on heuristic

Congenital heart disease: incidence and inheritance.

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The incidence of congenital heart disease

7 January 2021

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Targeted mutation of Cyln2 in the Williams syndrome critical region links CLIP-115 haploinsufficiency to neurodevelopmental abnormalities in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.TVJL.2005.02.007

Congenital heart diseases in small animals: part I. Genetic pathways and potential candidate genes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.TVJL.2005.02.007

The natural clinical history of canine congenital subaortic stenosis

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.TVJL.2005.02.007

Tricuspid atresia and annular hypoplasia: report of a familial occurrence

7 January 2021

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Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

7 January 2021

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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

7 January 2021

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Epidemiology of cardiovascular malformations: prevalence and risk factors

7 January 2021

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X-linked laterality sequence: situs inversus, complex cardiac defects, splenic defects.

7 January 2021

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Human genetics: dissecting Williams syndrome

7 January 2021

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Sex linked valvular dysplasia

7 January 2021

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Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

7 January 2021

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Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12

7 January 2021

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Molecular pathways controlling heart development

7 January 2021

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Epidemiologic and genetic studies of congenital heart disease in the dog

7 January 2021

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Hereditary defects of the conotruncal septum in Keeshond dogs: pathologic and genetic studies.

7 January 2021

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Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

7 January 2021

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Congenital heart disease caused by mutations in the transcription factor NKX2-5

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.TVJL.2005.02.007

A genetic blueprint for cardiac development

7 January 2021

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DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin

7 January 2021

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7 January 2021

Identifiers

DOI

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14 August 2017

1 reference