Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis (Q72097755)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7691712%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis (English)

1 reference

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23 October 2019

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H Sereth

1

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23 October 2019

T Shoshani

series ordinal

2

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23 October 2019

N Bashan

series ordinal

3

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23 October 2019

B S Kerem

series ordinal

4

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23 October 2019

publication date

1 October 1993

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23 October 2019

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23 October 2019

volume

92

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23 October 2019

issue

3

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23 October 2019

page(s)

289-295

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https://scigraph.springernature.com/pub.10.1007/bf00244474

23 October 2019

exact match

0 references

cites work

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

12 December 2020

Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease

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Ethnic variation in genetic disease: possible roles of hitchhiking and epistasis

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequences.

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Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis.

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Rapid nonradioactive detection of the major cystic fibrosis mutation.

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12 December 2020

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

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12 December 2020

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

1 reference

12 December 2020

Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG)

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12 December 2020

Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8.

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12 December 2020

A mutation in the second nucleotide binding fold of the cystic fibrosis gene.

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12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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12 December 2020

A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews

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12 December 2020

A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin

1 reference

12 December 2020

Identification of the cystic fibrosis gene: genetic analysis

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12 December 2020

Why is the cystic fibrosis gene so frequent?

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12 December 2020

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

12 December 2020

A tetranucleotide repeat polymorphism in the cystic fibrosis gene

1 reference

12 December 2020

The mutational specificity of DNA polymerase-beta during in vitro DNA synthesis. Production of frameshift, base substitution, and deletion mutations.

1 reference

12 December 2020

Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortium

1 reference

12 December 2020

Detection of over 98% cystic fibrosis mutations in a Celtic population

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00244474

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7691712%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

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