Evidence map›Paper›PMID 39080191›Full record

ArticleWorld journal of pediatrics : WJP2024

FLNB haploinsufficiency-related short stature: a new syndrome or an expanded spectrum of Larsen syndrome.

Qing Wang, Hong-Ying Wang, Shui-Yan Wu, Xue-Qian Wang, Hai-Ying Wu, Rong-Rong Xie, Feng-Yun Wang, Xiu-Li Chen, Lin-Qi Chen, Hai-Tao Lv and 1 more

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in World journal of pediatrics : WJP, 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

11 authors.

Qing WangDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Hong-Ying WangSuzhou Clinical Center for Rare Diseases in Children, Children's Hospital of Soochow University, Suzhou, China.
Shui-Yan WuIntensive Care Unit, Children's Hospital of Soochow University, Suzhou, China.
Xue-Qian WangSuzhou Clinical Center for Rare Diseases in Children, Children's Hospital of Soochow University, Suzhou, China.
Hai-Ying WuDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Rong-Rong XieDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Feng-Yun WangDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Xiu-Li ChenDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Lin-Qi ChenDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China.
Hai-Tao LvSuzhou Clinical Center for Rare Diseases in Children, Children's Hospital of Soochow University, Suzhou, China.
Ting ChenDepartment of Endocrinology, Genetics and Metabolism, Children's Hospital of Soochow University, Suzhou, China. chenting888@suda.edu.cn.ORCID 0000-0003-0155-0808

Funding

Jiangsu Commission of Health M2021082Jiangsu Provincial Maternal and Child Health Care Program F202119Science and Technology Program of Suzhou SKY2023007Summit Project of Clinical Medicine ML13100523Suzhou Clinical Center for Rare Disease Szlcyxzxj202105Suzhou Personnel Planning Project GSWS2020046
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DwarfismHaploinsufficiencyLaron SyndromeChildChild, PreschoolFemaleHumansMale

Identifiers

PMID39080191

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.