Evidence map›Paper›PMID 30214739›Full record

ArticleClinical case reports2018

A de novo derivative Y chromosome (partial Yq deletion and partial duplication of Yp and Yq) in a female with disorders of sex development.

Qing-Song Liu, Xing-Chun Zhu, Qiang Ma, Cheng He, Jian-Lan Shao

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

5 authors at 1 institution in 1 country.

Qing-Song LiuDepartment of Clinical Laboratory Affiliated Hospital of North Sichuan Medical College Nanchong Sichuan China.ORCID 0000-0003-3871-1169
Xing-Chun ZhuPathogenic Biology and Immunology Experiment Teaching Center North Sichuan Medical College Nanchong Sichuan China.
Qiang MaDepartment of Clinical Laboratory Affiliated Hospital of North Sichuan Medical College Nanchong Sichuan China.
Cheng HeDepartment of Clinical Laboratory Affiliated Hospital of North Sichuan Medical College Nanchong Sichuan China.
Jian-Lan ShaoDepartment of Obstetrics and Gynecology Affiliated Hospital of North Sichuan Medical College Nanchong Sichuan China.
North Sichuan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report an atypical disorders of sex development (DSD) case with no mutation of SYR gene but partial Yq deletion and partial duplication of Yp and Yq. This case emphasizes duplicated region Yp11.2→Yq11.223 with partial deletion of Yq11.223→Yqter most probably perturbed the sex differentiation and led to female phenotype.

Indexed as

disorders of sex developmentkaryotypeSRY

Identifiers

PMID30214739
PMCPMC6132170
OpenAlexW2858098268

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.