Evidence map›Paper›PMID 30719288›Full record

ArticleBiomedical reports2019

Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome.

Anh Lan Thi Luong, Thuong Thi Ho, Ha Hoang, Trung Quang Nguyen, Tu Cam Ho, Phan Duc Tran, Thuy Thi Hoang, Nam Trung Nguyen, Hoang Ha Chu

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Biomedical reports, 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
0.5field-weighted citation impact, top 28% of its field
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, 5 citations in OpenAlex.

  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

9 authors at 2 institutions in 1 country.

Anh Lan Thi LuongHanoi Medical University, Kim Lien, Đong Đa, Ha Noi 10000, Vietnam.
Thuong Thi HoNational Key Laboratory of Gene Technology, Institute of Biotechnology, Cau Giay, Ha Noi 10000, Vietnam.
Ha HoangNational Key Laboratory of Gene Technology, Institute of Biotechnology, Cau Giay, Ha Noi 10000, Vietnam.
Trung Quang NguyenHanoi Medical University, Kim Lien, Đong Đa, Ha Noi 10000, Vietnam.
Tu Cam HoHanoi Medical University, Kim Lien, Đong Đa, Ha Noi 10000, Vietnam.
Phan Duc TranHanoi Medical University, Kim Lien, Đong Đa, Ha Noi 10000, Vietnam.
Thuy Thi HoangNational Key Laboratory of Gene Technology, Institute of Biotechnology, Cau Giay, Ha Noi 10000, Vietnam.
Nam Trung NguyenNational Key Laboratory of Gene Technology, Institute of Biotechnology, Cau Giay, Ha Noi 10000, Vietnam.
Hoang Ha ChuNational Key Laboratory of Gene Technology, Institute of Biotechnology, Cau Giay, Ha Noi 10000, Vietnam.
Vietnam Academy of Science and Technology · VNHanoi Medical University · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Crouzon syndrome is a rare autosomal dominant genetic disorder, which causes the premature fusion of the cranial suture. Fibroblast growth factor receptor 2 (FGFR2) mutations are well-known causatives of Crouzon syndrome. The current study aimed to assess the

Indexed as

craniosynostosisCrouzon syndromefibroblast growth factor receptor 2 mutationmolecular analysisVietnamese family case

Identifiers

PMID30719288
PMCPMC6350211
OpenAlexW2907004412

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.