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

Characterization of a de novo balanced 1;Y translocation in a phenotypically normal twin male infant.

Fertility and sterility - 1 Apr 2006

Hatzissevastou-Loukidou Hariklia, Kalemi Theodora G, Lambropoulos Alexandros F, Nikita Maria, Sotiridou Ellada, Tarlatzis Basil C, Kotsis Alexandros

Abstract excerpt

OBJECTIVE: To report a translocation between an autosome and the Y chromosome. DESIGN: Amniocentesis of a fetus because of mother's advanced age followed by karyotype and PCR analysis. SETTING: Tertiary health center. PATIENT(S): A phenotypically normal twin male infant. INTERVENTION(S): Karyotype with G and Q banding and amplification of testis-specific protein 1-Y and of azoospermia factor (AZF) a, AZFb, AZFc,...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to Chromosomes, Human, Y

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Phenotype

Share to Pregnancy

Share to Translocation, Genetic

Source

Identifiers

PMID: 16580398
DOI: 10.1016/j.fertnstert.2005.09.058

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of a de novo balanced 1;Y translocation in a phenotypically normal twin male infant.PMID 16580398Read ↗

Azoospermia Due to a Unique De Novo Balanced Reciprocal Translocation (Y;1) (q12;q25)Semantic proximity Read ↗

Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report.Semantic proximity Read ↗

Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case reportSemantic proximity Read ↗

Pseudodicentric 22;Y translocation transmitted through four generations of a large family without phenotypic repercussion.Semantic proximity Read ↗

Prenatal diagnosis of <i>de novo</i> X;autosome translocationsSemantic proximity Read ↗

Molecular and Clinical Characteristics of 26 Cases with Structural Y Chromosome AberrationsSemantic proximity Read ↗

Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocationSemantic proximity Read ↗

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

Transmission of an unbalanced (Y;1) translocation in Brittany, FranceSemantic proximity Read ↗

Sex reversal due to Xp disomy by t(X;Y)(p21;q11).Semantic proximity Read ↗

Whole-arm translocations between chromosome 1 and acrocentric G chromosomes are associated with a poor prognosis for spermatogenesis: two new cases and review of the literature.Semantic 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 ↗

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