Evidence map›Paper›PMID 24959024›Full record

ArticleIndian journal of human genetics2014

Split-hand/feet malformation in three tamilian families and review of the reports from India.

S Deepak Amalnath, Maya Gopalakrishnan, Tarun Kumar Dutta

Abstract read
In one paragraph

Article in Indian journal of human genetics, 2014. 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
–field-weighted citation impact
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.

  1. Article
  2. A case of atypical cleft hand - reported with ontogenetic review.Journal of clinical and diagnostic research : JCDR · 2014
    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

3 authors.

S Deepak AmalnathDepartment of Medicine, Jawaharlal Institute of Medical Education and Research, Pondicherry, India.
Maya GopalakrishnanDepartment of Medicine, Jawaharlal Institute of Medical Education and Research, Pondicherry, India.
Tarun Kumar DuttaDepartment of Medicine, Jawaharlal Institute of Medical Education and Research, Pondicherry, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Split-hand/foot malformation (SHFM) is a rare condition which can be either syndromic or nonsyndromic. We report three unrelated pedigrees, one with autosomal dominant (AD) inheritance and the other two with autosomal recessive (AR) pattern. We also briefly review the published reports from India.

Indexed as

Autosomal dominantautosomal recessiveectrodactylyIndiansplit-hand/foot malformation

Identifiers

PMID24959024
PMCPMC4065489

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.