ArticleInternational journal of legal medicine1992
Population genetics and forensic efficiency data of 4 AMPFLP's.
Article in International journal of legal medicine, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.
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.
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.
Who cites it
33 citing papers in PubMed, 115 citations in OpenAlex.
- Diagnosis of HIV infection from bloodstains by PCR. A further marker for identification.International journal of legal medicine · 1995Trial
- A new sequenced allelic ladder marker for D1S80 typing.Journal of human genetics · 2004Article
- D1S80 (pMCT118) allele frequencies in a Malay population sample from Malaysia.International journal of legal medicine · 1997Article
- Sequence variation of allele 27 at the D1S80 locus.International journal of legal medicine · 1997Article
- Genetic control of T cell receptor BJ gene expression in peripheral lymphocytes of normal and rheumatoid arthritis monozygotic twins.The Journal of clinical investigation · 1996Article
- Population studies of three AMPFLPs systems in a north Polish population.International journal of legal medicine · 1996Article
- High-resolution vertical PAGE: an alternative electrophoretic system with multiple forensic applications.International journal of legal medicine · 1996Article
- Polymorphism analysis of the VNTR locus D17S5 in central Spain.International journal of legal medicine · 1996Article
- Validation of the STR system FES/FPS for forensic purposes in an Austrian population sample.International journal of legal medicine · 1995Article
- Structure of new mutations in 2 STR systems.International journal of legal medicine · 1995Article
- Population genetic study from the Zagreb area using 3 STR systems.International journal of legal medicine · 1995Article
- Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain).International journal of legal medicine · 1995Article
- Phenotype differences of STRs in 7 human populations.International journal of legal medicine · 1995Article
- Frequency profiles of 3 STRs in a Turkish population.International journal of legal medicine · 1995Article
- Validation of mitochondrial DNA sequencing for forensic casework analysis.International journal of legal medicine · 1995Article
- Observation of null alleles apparently due to deletions.International journal of legal medicine · 1995Article
- The use of the STRs HUMTH01, HUMVWA31/A, HUMF13A1, HUMFES/FPS, HUMLPL in forensic application: validation studies and population data for Galicia (NW Spain).International journal of legal medicine · 1995Article
- D1S80 (pMCT118): analysis of 3 ethnic subpopulations living in Brussels.International journal of legal medicine · 1995Article
- PCR-amplification of D2S44 alleles.International journal of legal medicine · 1994Article
- Analysis of the VNTR locus D1S80 in a Japanese population.International journal of legal medicine · 1994Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Family studies were carried out in a population sample from north west Germany using 4 amplifiable VNTR polymorphic systems D1S80 (MCT118), ApoB, D17S30 (YNZ22) and COL2A1. Separation was carried out in polyacrylamide gels and visualised using silver staining. In family studies (n = 30) no evidence of new mutations was found. The population study of unrelated individuals (mothers and putative fathers) showed that all 4 systems were highly polymorphic and similar to other population studies. The combined exclusion chance was calculated to be approximately 99% and the combined discrimination index 1.5.10(-4). The Hardy-Weinberg equilibrium was checked by forming groups of alleles and no significant deviations could be found in all systems.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.