(Q41610188)

English

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

scientific article published on August 1, 1992

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scholarly article

1 reference

Europe PubMed Central

5 October 2017

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1511975

3 October 2022

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

familial hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1511975

3 October 2022

author name string

Y. L. Ko

1

1 reference

Europe PubMed Central

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3 October 2022

W. P. Lien

2

1 reference

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3 October 2022

J. J. Chen

3

1 reference

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3 October 2022

C. W. Wu

4

1 reference

Europe PubMed Central

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3 October 2022

T. K. Tang

5

1 reference

Europe PubMed Central

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3 October 2022

C. C. Liew

6

1 reference

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3 October 2022

language of work or name

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National Center for Biotechnology Information

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3 October 2022

publication date

1 August 1992

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5 October 2017

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Europe PubMed Central

5 October 2017

89

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5 October 2017

6

1 reference

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5 October 2017

597-601

1 reference

Europe PubMed Central

5 October 2017

https://scigraph.springernature.com/pub.10.1007/bf00221945

0 references

Myocardial ultrastructure in idiopathic hypertrophic subaortic stenosis. A study of operatively excised left ventricular outflow tract muscle in 14 patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

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/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of the human genome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

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/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete sequence and organization of the human cardiac beta-myosin heavy chain gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

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/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A computer program for linkage analysis of general human pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy. A review

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

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/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns and significance of distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy. A wide angle, two dimensional echocardiographic study of 125 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial characterization of the human beta-myosin heavy-chain gene which is expressed in heart and skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of human cardiac myosin heavy chain genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12

1 reference

https://pubmed.ncbi.nlm.nih.gov/1511975

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/1511975

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00221945

1 reference

Europe PubMed Central

5 October 2017

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0 references

1 reference

Europe PubMed Central

5 October 2017

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