Evidence map›Paper›PMID 30533380›Full record

ArticleLeukemia research reports2019

The rare translocation t(14;21)(q11;q22) detected in a Moroccan patient with T-cell acute lymphoblastic leukemia.

Z Takki Chebihi, A Belkhayat, E Chadli, L Hessissen, M El Khorassani, M El Kababri, A Kili, M Khattab, Y Bakri, N Dakka

Open access · goldAbstract read
In one paragraph

Article in Leukemia research reports, 2019. 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
0.2field-weighted citation impact, top 34% 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

10 authors at 1 institution in 1 country.

Z Takki ChebihiLaboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco.
A BelkhayatBIOLAB Laboratory, Rabat, Morocco.
E ChadliBIOLAB Laboratory, Rabat, Morocco.
L HessissenDepartment of Pediatric Hemato-Oncology, Children's Hospital of Rabat, Morocco.
M El KhorassaniDepartment of Pediatric Hemato-Oncology, Children's Hospital of Rabat, Morocco.
M El KababriDepartment of Pediatric Hemato-Oncology, Children's Hospital of Rabat, Morocco.
A KiliDepartment of Pediatric Hemato-Oncology, Children's Hospital of Rabat, Morocco.
M KhattabDepartment of Pediatric Hemato-Oncology, Children's Hospital of Rabat, Morocco.
Y BakriLaboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco.
N DakkaLaboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, Mohammed V University, Rabat, Morocco.
Mohammed V University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytogenetic studies of acute lymphoblastic leukemia have been at the forefront of research in the pathogenesis of cancer. The presence of recurring chromosomal abnormalities (either numeral or structural rearrangements) provides immediate clues to the genetic events leading to leukemia and many abnormalities have important prognostic significance. The rare translocation t(14,21)(q11.2;q22) has been described in pediatric T lineage ALL in only one case so far in 2000. The present study is a case report of an ALL case in which we found a t(14,21)(q11.2;q22) as a non random chromosomal abnormality among 70 analyzed pediatric ALL cases referred exclusively to BIOLAB Laboratory from the children hospital of Morocco.

Indexed as

Acute lymphoblastic leukemiaChildrenCytogenetic abnormalitiesMoroccoT(14;21)

Identifiers

PMID30533380
PMCPMC6260455
OpenAlexW2901170626

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.