(Q33677532)

28 July 2017

title

Evidence of a long QT founder gene with varying phenotypic expression in South African families (English)

1 reference

28 July 2017

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de Jager T

1

1 reference

28 July 2017

Corbett CH

2

1 reference

28 July 2017

Badenhorst JC

3

1 reference

28 July 2017

Brink PA

4

1 reference

28 July 2017

Corfield VA

5

1 reference

28 July 2017

language of work or name

English

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publication date

1 July 1996

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

33

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28 July 2017

issue

7

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28 July 2017

page(s)

567-573

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A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Evidence of genetic and phenotypic heterogeneity in the Romano-Ward syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

The 1993-94 Généthon human genetic linkage map

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Mapping of a gene for long QT syndrome to chromosome 4q25-27

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Efficacy of left cardiac sympathectomy in the treatment of patients with the long QT syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

28 July 2018

Q-T interval syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Familial hypercholesterolemia in South African Afrikaners. PvuII and StuI DNA polymorphisms in the LDL-receptor gene consistent with a predominating founder gene effect.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

The long QT syndrome. Prospective longitudinal study of 328 families

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Dinucleotide repeat polymorphism at the D11S860 locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

28 July 2018

The long Q-T syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Locus heterogeneity of autosomal dominant long QT syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Gene for progressive familial heart block type I maps to chromosome 19q13.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Easy calculations of lod scores and genetic risks on small computers

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050664

Detection of two TaqI polymorphisms in the VTR region of the human HRAS1 oncogene

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8818942

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8818942

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8818942

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.33.7.567

1 reference

28 July 2017

1 reference

28 July 2017

1 reference