Evidence map›Paper›PMID 42200062›Full record

ArticleFrontiers in medicine2026

Identification of EVC variants and the preimplantation genetic testing in a Chinese family.

Haiyan Luo, Zhen Guo, Yao Yu, Jia Chen, Qing Lu, Yan Yang, Ting Huang, Danping Liu, Wangli Nie, Wan Lu and 4 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in medicine, 2026. 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

14 authors.

Haiyan LuoJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Zhen GuoJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yao YuJiujiang Polytechnic University of Science and Technology, Gongqing, Jiangxi, China.
Jia ChenJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Qing LuJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yan YangJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Ting HuangJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Danping LiuJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Wangli NieJiujiang Maternal and Child Health Hospital, Jiujiang, Jiangxi, China.
Wan LuJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Bicheng YangJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Jun ZouJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yanqiu LiuJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.
Yongyi ZouJiangxi Maternal and Child Health Hospital, Nanchang, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fetal genetic skeletal disorders are common congenital anomalies with notable genetic and phenotypic heterogeneity. Genetic analysis plays an important role in the definitive diagnosis of these skeletal conditions. In the present study, we aimed to determine the causative genetic factors underlying fetal skeletal disorders with shortened limbs (femoral lengths <-2.0 standard deviations) detected by routine second-trimester prenatal ultrasonography in a Chinese family. Whole exome sequencing (WES) analysis identified

Indexed as

EVCEVC syndromepreimplantation genetic testingprenatal diagnosisWES

Identifiers

PMID42200062
PMCPMC13199245

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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.