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

Characteristics and clinical evaluation of X chromosome translocations

21 Dec 2023

Abstract excerpt

BACKGROUND: Individuals with X chromosomal translocations, variable phenotypes, and a high risk of live birth defects are of interest for scientific study. These characteristics are related to differential breakpoints and various types of chromosomal abnormalities. To investigate the effects of X chromosome translocation on clinical phenotype, a retrospective analysis of clinical data for patients with X...

Read the complete abstract on PubMed

Topics

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

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Sexual Differentiation and Disorders
Share to Sperm and Testicular Function

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

Source

Identifiers

PMID: 38129867
DOI: 10.1186/s13039-023-00669-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

Characteristics and clinical evaluation of X chromosome translocationsPMID 38129867Read ↗

Characteristics and mechanisms of X chromosome translocationSemantic proximity Read ↗

Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.Semantic proximity Read ↗

Characterisation, phenotypic manifestations and X-inactivation pattern in 14 patients with X-autosome translocations.Semantic proximity Read ↗

49, XXXYY: Parental Origin, Occurrence, and Clinical Phenotypes.Semantic proximity Read ↗

Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal Male External Genitalia and a Literature ReviewSemantic proximity Read ↗

Is the resulting phenotype of an embryo with balanced X-autosome translocation, obtained by means of preimplantation genetic diagnosis, linked to the X inactivation pattern?Semantic proximity Read ↗

Molecular cytogenetic analysis and genetic counseling: a case report of eight 46,XX males and a literature reviewSemantic proximity Read ↗

Triple X syndrome with rare phenotypic presentation.Semantic proximity Read ↗

Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH.Semantic proximity Read ↗

Mild Phenotype of Xq Deletion and 3q Duplication Associated with der(X)t(X;3)(q21.1;q22.1) without Loss of XIST Gene.Semantic proximity Read ↗

45,X karyotype in an infertile man: how is this possible?Semantic proximity Read ↗

Unbalanced X;14 Translocation Leading to Turner Syndrome Phenotype: a case report and review of literatureSemantic proximity Read ↗

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