A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.

doi:10.1093/humrep/16.1.59

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

Back to search

Article

A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.

Human reproduction (Oxford, England) - 1 Jan 2001

Cai T, Yu P, Tagle D A, Lu D, Chen Y, Xia J

Abstract excerpt

A de novo complex chromosomal rearrangement (CCR) involving chromosomes 7, 8 and 9 in a male carrier was ascertained through his healthy wife's recurrent spontaneous abortions. Six pregnancies over eight years resulted in four spontaneous abortions and two livebirths who died perinatally due to abnormal vital signs. Cytogenetic analyses utilizing high resolution chromosome banding technique showed a deletion of...

Topics

Abortion, Habitual
Adult
Chromosome Aberrations
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Congenital Abnormalities
Female
Fertility
Humans
In Situ Hybridization, Fluorescence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Infant, Newborn

Karyotyping

Male

Phenotype

Pregnancy

Translocation, Genetic

Source

Open in PubMed

Identifiers

PMID: 11139537
DOI: 10.1093/humrep/16.1.59

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.PMID 11139537Read ↗

De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature.Semantic proximity Read ↗

[Genetic analysis of carriers of complex chromosome rearrangement].Semantic proximity Read ↗

Genomic complexity and complex chromosomal rearrangements in genetic diagnosis: example from two emblematic cases on chromosome 7Semantic proximity Read ↗

Molecular cytogenetic characterization of a de novo mosaic supernumerary ring chromosome 7: report of a new patient.Semantic proximity Read ↗

Hereditary chromosomal 9 inversion (p22q13) 9 as a cause for recurrent pregnancy loss: a case report.Semantic proximity Read ↗

Assisted reproductive technology and complex chromosomal rearrangements: the limits of ICSISemantic proximity Read ↗

Retrospective analysis of clinical pregnancy outcomes in patients with chromosome 9 inversionSemantic proximity Read ↗

An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.Semantic proximity Read ↗

Balanced complex chromosome rearrangements: Reproductive aspects. A reviewSemantic proximity Read ↗

Pericentric inversion (Inv) 9 variant—reproductive risk factor or benign finding?Semantic proximity Read ↗

Molecular analysis of a complex chromosomal rearrangement and a review of familial casesSemantic proximity Read ↗

Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism.Semantic proximity Read ↗

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