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

Gene analysis in patients with premature ovarian failure or gonadal dysgenesis: a preliminary study.

Maturitas - 20 Aug 2007

Massad-Costa Ana Maria, da Silva Ismael Dale Cotrim Guerreiro, Affonso Regina, Soares José Maria, Nunes Márcia Gaspar, de Lima Geraldo Rodrigues, Baracat Edmund C

Abstract excerpt

OBJECTIVE: The aim of this study was to evaluate the presence of mutations in the coding region of the QM gene and fragile X in patients with premature ovarian failure and gonadal dysgenesis. METHODS: After approval by the local Ethics Committee, blood samples, in EDTA, of 100 normally ovulating...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Case-Control Studies
Share to Fragile X Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Polymorphism, Single-Stranded Conformational

Share to Primary Ovarian Insufficiency

Share to Ribosomal Proteins

Share to Tumor Suppressor Proteins

Source

Identifiers

PMID: 17566674
DOI: 10.1016/j.maturitas.2007.04.005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17566674-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Gene analysis in patients with premature ovarian failure or gonadal dysgenesis: a preliminary study.PMID 17566674Read ↗

Premature ovarian failure and FMR1 gene mutations: an update.Semantic proximity Read ↗

Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patientsSemantic proximity Read ↗

Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction.Semantic proximity Read ↗

A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28.Semantic proximity Read ↗

Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failureSemantic proximity Read ↗

Association between idiopathic premature ovarian failure and fragile X premutation.Semantic proximity Read ↗

Premature ovarian failure and FRAXA premutation: Positive correlation in a Brazilian survey.Semantic proximity Read ↗

Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).Semantic proximity Read ↗

Variable expression of the Fragile X Mental Retardation 1 (FMR1) gene in patients with premature ovarian failure syndrome is not dependent on number of (CGG)n triplets in exon 1.Semantic proximity Read ↗

Premature ovarian failure and fragile X premutation: a study on 45 women.Semantic proximity Read ↗

Microdeletions in FMR2 may be a significant cause of premature ovarian failure.Semantic proximity Read ↗

Fragile X premutation screening in women with premature ovarian failure.Semantic proximity Read ↗

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