Evidence map›Paper›PMID 39175233›Full record

ArticleThe Journal of international medical research2024

Prenatal diagnosis and genetic counseling of a

Liu Ouyang, Yan Li, Fangfang Liu, Qin Zeng

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in The Journal of international medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Liu OuyangDepartment of Obstetrics, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, PR China.
Yan LiDepartment of Obstetrics, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, PR China.
Fangfang LiuDepartment of Obstetrics, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, PR China.
Qin ZengDepartment of Obstetrics, Renmin Hospital, Hubei University of Medicine, Shiyan, Hubei, PR China.ORCID 0009-0002-2466-1527

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copy number variants (CNVs) are an important source of normal and pathogenic genome variations. Unbalanced chromosome abnormalities are either gains or losses of large genomic regions that do not or only minimally clinically affect the individual. Noninvasive prenatal testing (NIPT) is widely used in the screening of common fetal chromosome aneuploidy. One example is the duplication of 10q11.21q11.23, which includes the 10q11.2 region. This region contains a complex set of low-copy repeats that may lead to various genomic alterations through non-allelic homologous recombination. In this report, we present a case of a

Indexed as

Chromosome DuplicationDNA Copy Number VariationsGenetic CounselingPhenotypePrenatal DiagnosisAdultChromosomes, Human, Pair 10FemaleHumansKaryotypingNoninvasive Prenatal TestingPregnancyUltrasonography, Prenatalchromosomal deletionchromosomal duplicationCopy number variantnoninvasive prenatal testingprenatal diagnosisunbalanced chromosome abnormality

Identifiers

PMID39175233
PMCPMC11344892

What OpenQuestion holds

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Registered trials

None linked

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.