ReviewJournal of medical genetics1992
Genetic deafness.
Review in Journal of medical genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 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
16 citing papers in PubMed.
- The Inheritance of Hearing Loss and Deafness: A Historical Perspective.Audiology research · 2024Review
- Global Research on Hereditary Hearing Impairment Over the Last 40 Years: A Bibliometric Study.The journal of international advanced otology · 2021Review
- A Rare Mutation in theInternational medical case reports journal · 2020Article
- Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2014Article
- Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment.European journal of pediatrics · 2009Article
- Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening: identification of two novel PDS/SLC26A4 mutations.European journal of pediatrics · 2008Article
- Chudley McCullough syndrome.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2008Review
- Cognition in children with sensorineural hearing loss: etiologic considerations.The Laryngoscope · 2007Article
- Hearing loss and connexin 26.Journal of the Royal Society of Medicine · 2002Review
- Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.Journal of medical genetics · 1999Article
- Article
- The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.American journal of human genetics · 1998Article
- An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.American journal of human genetics · 1996Article
- Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.American journal of human genetics · 1996Article
- A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.Journal of medical genetics · 1995Article
- Prevalence of selected congenital anomalies in Saudi children: a community-based study.Annals of Saudi medicineArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
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.