(Q35200623)

English

The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4.

scientific article published in 1986

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3004205%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

The analysis of multiple polymorphic loci on a single human chromosome to exclude linkage to inherited disease: cystic fibrosis and chromosome 4 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3004205%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

cystic fibrosis

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Peter J Scambler

2

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8 October 2019

author name string

Farrall M

1

1 reference

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8 October 2019

North P

3

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8 October 2019

Williamson R

4

1 reference

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8 October 2019

language of work or name

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publication date

1 January 1986

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8 October 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

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8 October 2019

38

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8 October 2019

75-83

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8 October 2019

1

1 reference

Europe PubMed Central

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8 October 2019

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Sequential tests for the detection of linkage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Multiple alleles in cystic fibrosis?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Mutations at more than one locus may be involved in cystic fibrosis--evidence based on first-cousin data and direct counting of cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Genetic linkage between structural loci for albumin and group specific component (Gc)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

An unusual human serum albumin variant: further data on genetic linkage between loci for human serum albumin and group-specific component (Ge).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

A search for linkage in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

A computer program for linkage analysis of general human pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

A maximum likelihood map of chromosome 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Evolution of sickle variant gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

13 July 2018

Retraction: No evidence for more than one locus in cystic fibrosis .

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684714

26 September 2018

The use of lod scores for the determination of the order of loci on a chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MNSs blood groups of families with chromosome 4 rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion mapping illustrated by the MNSs blood group

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis is not caused by a defect in the gene coding for human complement C3

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal linkage between the albumin and Gc loci in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/3004205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3004205%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3004205%20AND%20SRC:MED&resulttype=core&format=json

8 October 2019

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