ReviewHuman genetics1987
Diagnosis of genetic disease using recombinant DNA. Supplement.
Review in Human genetics, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 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
13 citing papers in PubMed, 27 citations in OpenAlex.
- Influence of mosaicism on sexing of human preembryos detected by the polymerase chain reaction.Journal of assisted reproduction and genetics · 1996Article
- Sodium chloride deficiency in cystic fibrosis patients.European journal of pediatrics · 1994Article
- Diagnosis of human genetic disease using recombinant DNA. Fourth edition.Human genetics · 1993Review
- Diagnosis of genetic disease using recombinant DNA. Third edition.Human genetics · 1991Review
- Diagnosis of genetic disease using recombinant DNA. Second edition.Human genetics · 1989Review
- Genetic analysis of DNA from single human oocytes: a model for preimplantation diagnosis of cystic fibrosis.BMJ (Clinical research ed.) · 1989Article
- Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome.Human genetics · 1989Article
- Evidence that the familial adenomatous polyposis gene is involved in a subset of colon cancers with a complementable defect in c-myc regulation.Proceedings of the National Academy of Sciences of the United States of America · 1989Article
- DNA sampling and informed consent.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 1989Article
- DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases.Human genetics · 1989Article
- Start a DNA diagnostic service.BMJ (Clinical research ed.) · 1988Article
- DNA polymorphism and the study of disease associations.Human genetics · 1988Review
- The CpG dinucleotide and human genetic disease.Human genetics · 1988Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recombinant DNA methodology has greatly increased our knowledge of the molecular pathology of the human genome at the same time as providing the means to diagnose inherited disease as the DNA level. We present here a list of recent reports of both direct and indirect analysis of human inherited disease which is intended to serve as a guide to current molecular genetic approaches to diagnostic medicine.
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.