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 role of genes in the development of Mullerian anomalies: where are we today?

Obstetrical & gynecological survey - 1 Nov 2009

Christopoulos Panagiotis, Gazouli Maria, Fotopoulou Georgia, Creatsas George

Abstract excerpt

UNLABELLED: Recent studies claim that researchers are challenged to find out the pathogenesis of the congenital anomalies of the female reproductive tract. Their frequency is estimated to be between 0.1% and 3% of live births in humans. During the experiments a number of genes were detected to contribute to the formation and development of the female reproductive tract. This review article aims to report these...

Read the complete abstract on PubMed

Topics

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

Share to Amenorrhea
Share to Anti-Mullerian Hormone
Share to Genitalia, Female

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Mullerian Ducts

Share to PAX2 Transcription Factor

Share to Proto-Oncogene Proteins

Share to Wnt Proteins

Source

Identifiers

PMID: 19849868
DOI: 10.1097/OGX.0b013e3181bea203

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of genes in the development of Mullerian anomalies: where are we today?PMID 19849868Read ↗

Unraveling the Genetic Mysteries of Müllerian Anomalies: Research Approaches and Clinical Significance.Semantic proximity Read ↗

Genetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene TherapySemantic proximity Read ↗

Studying Müllerian duct anomalies - from cataloguing phenotypes to discovering causation.Semantic proximity Read ↗

Molecular Basis of Mullerian Agenesis Causing Congenital Uterine Factor Subfertility- a Systematic ReviewSemantic proximity Read ↗

Genetics of the female reproductive ductsSemantic proximity Read ↗

Molecular Genetics of Müllerian Duct Formation, Regression and DifferentiationSemantic proximity Read ↗

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

Müllerian anomalies and endometriosis: associations and phenotypic variations.Semantic proximity Read ↗

Genetics of anti-Müllerian hormone and its signaling pathwaySemantic proximity Read ↗

Mechanistic Drivers of Müllerian Duct Development and Differentiation Into the OviductSemantic proximity Read ↗

The genetic basis of female reproductive disorders: Etiology and clinical testingSemantic proximity Read ↗

Clinical aspects and molecular genetics of the persistent müllerian duct syndrome.Semantic proximity Read ↗

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