(Q35442640)

8 August 2017

title

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

1 reference

8 August 2017

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G Andelfinger

1

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8 August 2017

K N Wright

2

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8 August 2017

H S Lee

3

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8 August 2017

L M Siemens

4

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8 August 2017

D W Benson

5

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8 August 2017

language of work or name

English

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publication date

1 May 2003

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Journal of Medical Genetics

8 August 2017

published in

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8 August 2017

volume

40

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8 August 2017

issue

5

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8 August 2017

page(s)

320-324

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Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Unleashing the canine genome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Genetic mapping of a naturally occurring hereditary renal cancer syndrome in dogs

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Canine genetics comes of age.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Retrospective study of congenital heart defects in 151 dogs

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Ebstein's malformation of the tricuspid valve: genetic and environmental factors. The Baltimore-Washington Infant Study Group

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Left-sided anomalies in Ebstein's malformation of the tricuspid valve

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Familial Ebstein's anomaly: a report of six cases in two generations associated with mild skeletal abnormalities

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Ebstein's anomaly. Genetic study of 26 families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Ebstein's anomaly: a report of 3 cases in the dog.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Morphologic spectrum of Ebstein's anomaly of the heart: a review

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Left ventricular anomalies associated with Ebstein's malformation of the tricuspid valve

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Dysplasia of the tricuspid valve in the dog and cat

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Identification of a premature stop codon in the melanocyte-stimulating hormone receptor gene (MC1R) in Labrador and Golden retrievers with yellow coat colour

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Avoiding recomputation in linkage analysis.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735483

Characterization of a minimal screening set of 172 microsatellite markers for genome-wide screens of the canine genome

26 September 2018

1 reference

12 December 2020

Meiotic linkage mapping of 52 genes onto the canine map does not identify significant levels of microrearrangement

1 reference

12 December 2020

Familial ebstein's anomaly with emphasis on the surgical treatment

1 reference

12 December 2020

Four Cases of Congenital Malformation of the Heart in a Litter of Eleven Dogs

1 reference

12 December 2020

Familial Ebstein's anomaly

1 reference

12 December 2020

Multiple cardiac anomalies in a family of Saluki dogs

1 reference

12 December 2020

Angiographic and morphologic features of the left ventricle in Ebstein's malformation

1 reference

12 December 2020

A large pedigree with valvuloseptal defects

1 reference

12 December 2020

Atrioventricular valve dysplasia in dalmatians

1 reference

12 December 2020

Ebstein anomaly associated with rearrangements of chromosomal region 11q

1 reference

12 December 2020

Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder

1 reference

12 December 2020

Familial protein-losing enteropathy and protein-losing nephropathy in Soft Coated Wheaten Terriers: 222 cases (1983-1997)

1 reference

12 December 2020

[Tricuspid valve dysplasia in fifteen dogs]

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.40.5.320

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8 August 2017

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8 August 2017

1 reference