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Article

[The frequency of F508 deletion of the mucoviscidosis gene in patients and in families at high risk in Soviet populations].

Doklady Akademii nauk SSSR - 1 Jan 1990

Baranov V S, Ivashchenko T E, Gorbunova V N, Dean M

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 7
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 2149699

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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[The frequency of F508 deletion of the mucoviscidosis gene in patients and in families at high risk in Soviet populations].PMID 2149699Read ↗

[Repartition of frequency of main mutation (delta F508) in mucoviscidosis in France: results of multicenter study of 1030 unrelated families].Semantic proximity Read ↗

[An analysis of the mutations in the mucoviscidosis gene: the origin and distribution of the delF508 major mutation in Ukraine].Semantic proximity Read ↗

[Frequency of the main mutation (delta F508) of cystic fibrosis in France: new results about 1656 unrelated families].Semantic proximity Read ↗

[The mutation spectrum of the CFTR gene in mucoviscidosis patients from Bashkortostan].Semantic proximity Read ↗

[Use of molecular DNA probes in the diagnosis of mucoviscidosis-- analysis of restriction fragment length polymorphisms (RFLP) in 22 high-risk families].Semantic proximity Read ↗

[An analysis of mutations in the 7th, 10th and 11th exons and of the polymorphism of the 4 nucleotide tandem repeats from the 3' end of the 6th intron of the CFTR gene in families from Ukraine with a high risk of mucoviscidosis].Semantic proximity Read ↗

[Prenatal diagnosis of mucoviscidosis: indication of enzyme determination and molecular biology techniques].Semantic proximity Read ↗

[Is mucoviscidosis transmited by a recessive autosomal gene?].Semantic proximity Read ↗

[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene].Semantic proximity Read ↗

[Allele polymorphism of the DNA loci MET, D7S8, D7S23, linked to the cystic fibrosis gene in some populations of the USSR, in high risk families and in cystic fibrosis patients].Semantic proximity Read ↗

[Polymorphism of nucleotide sequences of human genomic DNA linked to a mucoviscidosis locus].Semantic proximity Read ↗

[Determination of the frequency of the deltaF508 mutation among newborns in the city of Moscow and evaluation of the frequency of cystic fibrosis in the European part of Russia].Semantic proximity Read ↗

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