(Q40575361)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

title

Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

1 reference

R G Knowlton

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

E J Weaver

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

A F Struyk

3

1 reference

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1 October 2019

W H Knobloch

4

1 reference

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1 October 2019

R A King

5

1 reference

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1 October 2019

K Norris

6

1 reference

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1 October 2019

A Shamban

7

1 reference

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1 October 2019

J Uitto

8

1 reference

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1 October 2019

S A Jimenez

9

1 reference

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1 October 2019

D J Prockop

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

language of work or name

English

0 references

publication date

1 November 1989

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

1 October 2019

published in

1 reference

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1 October 2019

volume

45

1 reference

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1 October 2019

issue

5

1 reference

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1 October 2019

page(s)

681-688

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY

1 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Strategies for multilocus linkage analysis in humans

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Heritable diseases of collagen

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

A highly polymorphic region 3' to the human type II collagen gene.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Isolation and partial characterization of genomic clones coding for a human pro-alpha 1 (II) collagen chain and demonstration of restriction fragment length polymorphism at the 3' end of the gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

A highly polymorphic locus in human DNA revealed by cosmid-derived probes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Isolation and partial characterization of the entire human pro alpha 1(II) collagen gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Isolation and mapping of a polymorphic DNA sequence pYNH15 on chromosome 12q [D12S17]

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Inherited hyaloideoretinopathy and skeletal dysplasia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

The Stickler syndrome (hereditary arthroophthalmopathy)

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Clefting syndromes associated with retinal detachment.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplantation

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

A primary genetic linkage map for human chromosome 12.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

International nosology of heritable disorders of connective tissue, Berlin, 1986

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683441

Hereditary progressive arthro-ophthalmopathy of Stickler

2 December 2018

1 reference

12 December 2020

The Wagner-Stickler syndrome: A study of 22 families

1 reference

12 December 2020

A test of the role of two oncogenes in inherited predisposition to colon cancer

1 reference

12 December 2020

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2573273%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

PubMed publication ID

2573273

1 reference