Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[The use of DNA analysis for diagnostics of hereditary premature ovarian failure].

TSitologiia i genetika - 1 Jan 2000

Livshyts' H B, Kravchenko S A, Hryshchenko N V, Sudoma I A

Abstract excerpt

Methods of DNA-analysis of 769G --> A mutations in INHalpha1 gene and CGG-repeats polymorphism in FMRI gene have been developed for creating test-systems for genetically caused forms of premature ovarian failure (POF) diagnostics. The frequency of 769G --> A mutation among women population in Ukraine was established and, by preliminary calculations, makes up 2.8%. Results of analysis of CGG-repeats numbers in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fragile X Mental Retardation Protein
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Inhibins

Share to Nerve Tissue Proteins

Share to Polymorphism, Restriction Fragment Length

Share to Primary Ovarian Insufficiency

Share to RNA-Binding Proteins

Share to Trinucleotide Repeat Expansion

Source

Identifiers

PMID: 16161415

Genes

FMR1

Provenance

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→

Click a neighbor to travelStep 1 · 12 closest

[The use of DNA analysis for diagnostics of hereditary premature ovarian failure].PMID 16161415Read ↗

[Molecular-genetic analysis of natural and stimulated ovulation impairment].Semantic proximity Read ↗

Association analysis of FMR1 genetic variants and primary ovarian insufficiency in South Indian women with a novel approach of CGG repeats classification.Semantic proximity Read ↗

[Allelic polymorphism of FMR1 gene CGG-repeat region in patients with impairment of natural and stimulated ovulation].Semantic proximity Read ↗

[Triplet expansion cytosine-guanine-guanine: Three cases of OMIM syndrome in the same family].Semantic proximity Read ↗

[DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR].Semantic proximity Read ↗

Implications of the FMR1 gene in menopause: study of 147 Spanish women.Semantic proximity Read ↗

Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations.Semantic proximity Read ↗

[Possibilities and prospects of the use of DNA analysis in the diagnosis and prevention of inherited disease in the Ukraine].Semantic proximity Read ↗

[A case pf spontaneous deletion in the FMR1 gene in a patient with the Martin-Bell syndrome].Semantic proximity Read ↗

Controversial role of inhibin α-subunit gene in the aetiology of premature ovarian failureSemantic 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 ↗

[Prevention of fragile X syndrome by prenatal genetic diagnosis: advantages and controversial aspects].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.