(Q41887818)

13 October 2017

A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. (English)

1 reference

13 October 2017

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Wainwright B

1

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13 October 2017

Farrall M

series ordinal

2

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13 October 2017

Watson E

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3

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13 October 2017

Williamson R

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4

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13 October 2017

language of work or name

English

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publication date

1 October 1986

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Journal of Medical Genetics

13 October 2017

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13 October 2017

23

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13 October 2017

417-420

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13 October 2017

5

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Assignment of the structural gene for the third component of human complement to chromosome 19.

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Strategies for multilocus linkage analysis in humans

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

The isolation and characterization of cDNA clones for human apolipoprotein CII.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

A polymorphic DNA marker genetically linked to Huntington's disease

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Possible localisation of the gene for cystic fibrosis of the pancreas to the short arm of chromosome 5.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

RFLP for a human cytochrome P-450 gene at 19q13.1-qter (HGM8 provisional designation CYPI)

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Incidence in Italy, genetic heterogeneity, and segregation analysis of cystic fibrosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Isolation and sequence of a human cytochrome P-450 cDNA clone

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

The structural gene for human coagulation factor X is located on chromosome 13q34

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049778

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

3 November 2018

1 reference

12 December 2020

Somatic cell genetic studies of the cystic fibrosis mucociliary inhibitor

1 reference

12 December 2020

Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis

1 reference

12 December 2020

A DNA polymorphism adjacent to the human apolipoprotein CII gene

1 reference

12 December 2020

Localisation of genetic markers and orientation of the linkage group on chromosome 19

1 reference

12 December 2020

A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis

1 reference

12 December 2020

Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications.

1 reference

12 December 2020

A closely linked genetic marker for cystic fibrosis

1 reference

12 December 2020

Localization of cystic fibrosis locus to human chromosome 7cen–q22

1 reference

12 December 2020

Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis

1 reference

12 December 2020

Identifiers

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1 reference

13 October 2017

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