(Q34333065)

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Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12.

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12. (English)

1 reference

Europe PubMed Central

1 August 2017

congenital disorder

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congenital fibrosis of the extraocular muscles

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author name string

Engle EC

1

1 reference

Europe PubMed Central

1 August 2017

Kunkel LM

2

1 reference

Europe PubMed Central

1 August 2017

Specht LA

3

1 reference

Europe PubMed Central

1 August 2017

Beggs AH

4

1 reference

Europe PubMed Central

1 August 2017

language of work or name

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publication date

1 May 1994

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Europe PubMed Central

1 August 2017

Nature Genetics

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Europe PubMed Central

1 August 2017

7

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Europe PubMed Central

1 August 2017

1

1 reference

Europe PubMed Central

1 August 2017

69-73

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Europe PubMed Central

1 August 2017

https://scigraph.springernature.com/pub.10.1038/ng0594-69

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Joubert's syndrome associated with congenital ocular fibrosis and histidinemia.

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

21 January 2018

Histochemistry of human extraocular muscle

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Motor innervation and acetylcholine receptor distribution of human extraocular muscle fibres

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Extraocular muscles are spared in advanced Duchenne dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital general fibrosis of the extraocular muscles

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary congenital external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital fibrosis of the extraocular muscles; a report of six cases

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Dinucleotide repeat polymorphism at the GABAA receptor beta 3 (GABRB3) locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

A second-generation linkage map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the first international workshop on human chromosome 12 mapping.

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of a gene which complements branched-chain amino acid transaminase deficiency to the short arm of human chromosome 12

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

3,400 new expressed sequence tags identify diversity of transcripts in human brain

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Strabismus fixus

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Bilateral vertical retraction syndrome. A family study

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://api.crossref.org/works/10.1038%2FNG0594-69

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0594-69

1 reference

Europe PubMed Central

1 August 2017

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1 reference

Europe PubMed Central

1 August 2017

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