Evidence map›Paper›PMID 40628998›Full record

ArticleEuropean journal of human genetics : EJHG2026

Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family.

Ting Wen, Gulsen Akay, Janice Palumbos, Betsy Ostrander, Denise I Quigley, Allen N Lamb, Erica F Andersen, Bo Hong, David Viskochil

Abstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. New year, new insights in genomic medicine.European journal of human genetics : EJHG · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ting Wen *Department of Pathology, University of Utah, Salt Lake City, UT, USA. twen1@hfhs.org.ORCID 0009-0006-7209-5565
Gulsen Akay *Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
Janice PalumbosDivision of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
Betsy OstranderDivision of Pediatric Neurology, Department of Pediatrics University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID 0009-0002-4400-4217
Denise I QuigleyARUP Laboratories, Salt Lake City, UT, USA.
Allen N LambARUP Laboratories, Salt Lake City, UT, USA.
Erica F AndersenDepartment of Pathology, University of Utah, Salt Lake City, UT, USA.
Bo HongDepartment of Pathology, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0003-1004-0172
David ViskochilDivision of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA. Dave.Viskochil@hsc.utah.edu.ORCID 0000-0001-5364-3366

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carriers of balanced pericentric inversions are at risk for producing unbalanced gametes because of meiotic recombination resulting in de novo deletion and duplication of distal chromosome ends. Recombinant chromosomes generally lead to significant imbalances resulting in anomalous clinical phenotypes in offspring, hence they are typically not inherited. Therefore, the vertical transmission of recombinant chromosomes is a clinically rare event. Using genomic microarray and karyotyping, we describe inheritance of recombinant chromosomes in a three-generation family with the grandmother carrying a mosaic pericentric inversion of chromosome 18. Three children inherited the balanced inversion and one child with a mild phenotype inherited a de novo recombinant chromosome 18. In the third generation, a newborn with a variant of holoprosencephaly inherited an unmodified recombinant chromosome from her mother. Despite having the same karyotype predicting loss of the TGIF1 gene from the 18p terminus, the mother exhibits a relatively unaffected phenotype. The cousin of the child with holoprosencephaly carries the reciprocal recombinant chromosome 18 with a much milder phenotype. We verified the cytogenetic mechanism and corresponding clinical phenotypes in affected individuals and illustrated possible recombinant chromosome consequences of the inversion of chromosome 18 in this three-generation family.

Indexed as

Chromosome InversionChromosomes, Human, Pair 18HoloprosencephalyPhenotypeRecombination, GeneticAdultChildFemaleHomeodomain ProteinsHumansInfant, NewbornMalePedigreeRepressor ProteinsHomeodomain ProteinsRepressor Proteins

Identifiers

PMID40628998
PMCPMC12816133

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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.