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

Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism.

Climacteric : the journal of the International Menopause Society - 1 Apr 2011

Gersak K, Franic D, Veble A, Pajnic I Zupanic, Teran N, Writzl K

Abstract excerpt

Genetic causes of premature ovarian failure (POF) comprise less than one-third of all cases, among them X chromosome abnormalities, mutations and polymorphisms in some genes. The frequency of X-chromosome mosaicism in women with sporadic POF has been found to range between 3 and 10%, whereas the prevalence of POF in carriers of the FMR1 premutation is estimated to range between 13 and 25%. We report two...

Read the complete abstract on PubMed

Topics

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

Share to Chimerism
Share to Chromosomes, Human, X

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

Share to Embryo Transfer

Share to Fertilization in Vitro

Share to Fragile X Mental Retardation Protein

Share to Lymphocytes

Share to Mosaicism

Share to Primary Ovarian Insufficiency

Source

Identifiers

PMID: 20575655
DOI: 10.3109/13697137.2010.490604

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

Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism.PMID 20575655Read ↗

Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure.Semantic proximity Read ↗

Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.Semantic proximity Read ↗

Premature ovarian insufficiency: clinical orientations for genetic testing and genetic counselingSemantic proximity Read ↗

FMR1 and the continuum of primary ovarian insufficiency.Semantic proximity Read ↗

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene.Semantic proximity Read ↗

A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency.Semantic proximity Read ↗

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

Genetics of female infertility due to anomalies of the ovary and mullerian ducts.Semantic proximity Read ↗

Premature ovarian failure and FMR1 premutation co-segregation in a large Brazilian family.Semantic proximity Read ↗

Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report.Semantic proximity Read ↗

Premature ovarian failure and the FMR1 gene.Semantic proximity Read ↗

Association between fragile X premutation and premature ovarian failure: a case-control study and meta-analysis.Semantic proximity Read ↗

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