Evidence map›Paper›PMID 37601716›Full record

ArticleActa endocrinologica (Bucharest, Romania : 2005)

RARE DOSAGE ABNORMALITIES - COPY NUMBER VARIATIONS FLANKING THE SHOX GENE.

I Gherlan, E Braha, D C Manole, L Radomir, I Nedelcu, O Popa, S Schipor

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PubMed Full text at PMC Publisher
In one paragraph

Article in Acta endocrinologica (Bucharest, Romania : 2005). 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
–field-weighted citation impact, top 81% 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, 0 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

7 authors at 1 institution in 1 country.

I GherlanPediatric Endocrinology Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
E BrahaResearch Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
D C ManolePediatric Endocrinology Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
L RadomirPediatric Endocrinology Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
I NedelcuResearch Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
O PopaResearch Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
S SchiporResearch Department, "C.I. Parhon" National Institute of Endocrinology Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Molecular defects in the Results: We describe two cases with short stature and normal GH-IGF1 status. Multiplex ligation-dependent probe amplification (MLPA) and array comparative genomic hybridization (arrayCGH) identified in both cases heterozygous duplications involving downstream regions of Conclusion: To our knowledge, these are the first Romanian-reported cases of ISS with a large duplication of downstream

Indexed as

CNEdeletionduplicationidiopathic short statureregulatory elementSHOX

Identifiers

PMID37601716
PMCPMC10439321
OpenAlexW4385639687

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.