(Q72720019)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

1 reference

Y L Ko

1

1 reference

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28 October 2019

S A Chen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

T K Tang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

J L Lin

4

1 reference

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28 October 2019

C E Chiang

5

1 reference

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28 October 2019

J J Chen

6

1 reference

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28 October 2019

M S Teng

7

1 reference

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28 October 2019

M S Chang

8

1 reference

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28 October 2019

W P Lien

9

1 reference

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28 October 2019

C W Wu

10

1 reference

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28 October 2019

publication date

1 October 1994

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28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

volume

94

1 reference

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28 October 2019

issue

4

1 reference

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28 October 2019

page(s)

364-366

1 reference

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No evidence for linkage of familial hypertrophic cardiomyopathy and chromosome 14q1 locus D14S26 in a Chinese family: evidence for genetic heterogeneity

28 October 2019

cites work

1 reference

12 December 2020

Linkage of tyrosine hydroxylase to four other markers on the short arm of chromosome 11.

1 reference

12 December 2020

Microsatellites for linkage analysis of genetic traits

1 reference

12 December 2020

Idiopathic long QT syndrome: progress and questions

1 reference

12 December 2020

Evidence of genetic heterogeneity in the long QT syndrome

1 reference

12 December 2020

The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences

1 reference

12 December 2020

Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Hypothesis for the molecular physiology of the Romano-Ward long QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Locus heterogeneity of autosomal dominant long QT syndrome

1 reference

12 December 2020

A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

1 reference

12 December 2020

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

1 reference

12 December 2020

RARE CARDIAC ARRYTHMIAS OF THE PEDIATRIC AGE. II. SYNCOPAL ATTACKS DUE TO PAROXYSMAL VENTRICULAR FIBRILLATION. (PRESENTATION OF 1ST CASE IN ITALIAN PEDIATRIC LITERATURE)

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00201594

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7927330%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference