Evidence map›Paper›PMID 10985005›Full record

ArticleIndian journal of pediatrics2000

Trisomy 4p and partial monosomy 18q due to paternal translocation t(4;18) (p11; q21.3).

G Thanemozhi, S T Santhiya, N Chandra, G Palka, S Jayam, P M Gopinath

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In one paragraph

Article in Indian journal of pediatrics, 2000. 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, top 90% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

6 authors at 3 institutions in 2 countries.

G ThanemozhiDepartment of Genetics, Dr. A.L.M. Post Graduate Institute of Basic Medical Sciences, University of Madras, Taramani, Chennai, India.
S T Santhiya
N Chandra
G Palka
S Jayam
P M Gopinath
University of Madras · INUniversity of Chieti-Pescara · ITVijaya Medical and Educational Trust · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A carrier status for balanced translocation in either of the parents increases the risk of congenital malformation in the offspring. A case of multiple congenital anomalies in a female newborn was found to be associated with trisomy 4p and partial monosomy 18q as a result of a reciprocal translocation, t(4; 18) (p11; q21.3) in the father. The clinical and cytogenetic findings are compared with characteristic features of trisomy 4p, monosomy 18q and two similar cases reported earlier.

Indexed as

Chromosomes, Human, Pair 18Chromosomes, Human, Pair 4Translocation, GeneticAbnormalities, MultipleAdultChromosome AberrationsChromosome DisordersFathersFemaleFoot Deformities, CongenitalHeart Defects, CongenitalHumansIndiaInfant, NewbornIn Situ Hybridization, FluorescenceMonosomy

Identifiers

PMID10985005
OpenAlexW1964454068

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.