Evidence map›Paper›PMID 31544782›Full record

ArticleJournal of genetics2019

Developmental retardation due to paternal 5q/11q translocation in a Chinese infant: clinical, chromosomal and microarray characterization.

Xiangyu Zhao, Hongyan Xu, Chen Zhao, Lin Li

Abstract readCase Reports
PubMed
In one paragraph

Article in Journal of genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Xiangyu ZhaoDepartment of Medical Genetics, Linyi People's Hospital, Linyi 276003, Shandong, People's Republic of China. lilinxy1996@163.com.
Hongyan Xu
Chen Zhao
Lin Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although it is known that the parental carriers of chromosomal translocation are considered to be at high risk for spontaneous abortion and embryonic death, normal gestation and delivery remain possible. This study aims to investigate the genetic factors of a Chinese infant with multiple malformations and severe postnatal development retardation. In this study, the routine cytogenetic analysis, chromosomal microarray analysis (CMA) and fluorescence

Indexed as

Chromosomes, Human, Pair 11Translocation, GeneticAbnormalities, MultipleChromosome DeletionChromosome DuplicationChromosomes, Human, Pair 5Cytogenetic AnalysisDevelopmental DisabilitiesHumansInfantIn Situ Hybridization, FluorescenceIntellectual DisabilityKaryotypingMaleMicroarray AnalysisTrisomy

Identifiers

PMID31544782

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.