(Q71599194)

English

Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type

scientific article published on 01 April 1996

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scholarly article

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19 October 2019

Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type (English)

1 reference

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19 October 2019

hypertrophic cardiomyopathy

1 reference

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inferred from title

familial hypertrophic cardiomyopathy

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author name string

Y L Ko

1

1 reference

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19 October 2019

J J Chen

2

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19 October 2019

T K Tang

3

1 reference

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19 October 2019

M S Teng

4

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19 October 2019

S Y Lin

5

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19 October 2019

P Kuan

6

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19 October 2019

C W Wu

7

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19 October 2019

W P Lien

8

1 reference

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19 October 2019

C C Liew

9

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19 October 2019

publication date

1 April 1996

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19 October 2019

1 reference

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19 October 2019

97

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19 October 2019

457-461

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19 October 2019

4

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19 October 2019

https://scigraph.springernature.com/pub.10.1007/bf02267066

0 references

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apical hypertrophic cardiomyopathy: the continuing saga

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apical hypertrophic cardiomyopathy of the Japanese type: occurrence with familial hypertrophic cardiomyopathy in a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic hypertrophic cardiomyopathy in identical twins. Morphological heterogeneity of the left ventricle

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A tetranucleotide repeat for the F13B locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric apical hypertrophy: ten years experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic cardiomyopathy in identical twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of the chromosomal location of a gene responsible for hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneous morphologic expression of genetically transmitted hypertrophic cardiomyopathy. Two-dimensional echocardiographic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): Ventriculographic and echocardiographic features in 30 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A StuI RFLP in the human beta-spectrin gene (SPTB)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

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[Apical hypertrophy and its genetic and acquired factors]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inheritance of hypertrophic cardiomyopathy in Chinese--M-mode and two-dimensional echocardiographic analysis of 28 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear proteins of the bovine esophageal epithelium. II. The NuMA gene gives rise to multiple mRNAs and gene products reactive with monoclonal antibody W1

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8834242

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02267066

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8834242%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8834242%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

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