ArticleJournal of applied genetics2009
Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review.
Article in Journal of applied genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed, 14 citations in OpenAlex.
- Complex chromosomal rearrangements induce embryonic chromosomal imbalance and significantly compromise reproductive outcomes.Contraception and reproductive medicine · 2026Article
- Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies.Journal of human genetics · 2024Article
- Chromosomal segregation analysis and HOST-based sperm selection in a complex reciprocal translocation carrier.Journal of assisted reproduction and genetics · 2023Article
- Identification of a familial complex chromosomal rearrangement by optical genome mapping.Molecular cytogenetics · 2022Article
- Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review.Frontiers in genetics · 2022Article
- A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.Journal of assisted reproduction and genetics · 2017Article
- Small supernumerary marker chromosome (sSMC) derived from chromosome 22 in an infertile man with hypogonadotropic hypogonadism.Journal of applied genetics · 2011Article
- Azoospermia related to a unique karyotype: 45,XY,-13,-19,+der(19)t(13;19)(q12;p13).Journal of applied genetics · 2011Article
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Here we describe a rare case of an apparently balanced karyotype of 46, XY, t(1;22;4)(p22.3;q11.1;q31.1) in a infertile male with oligoastenoteratozoospermia (OAT). He was the second patient with complex chromosomal rearrangement (CCR) referred to our center because of infertility. We also review reports on 24 males carrying CCRs with spermatogenesis failure or a malformed child, to provide information on the reproductive outcome of male CCR carriers.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.