ReviewMolecular medicine (Cambridge, Mass.)1998
Charcot-Marie-Tooth disease: lessons in genetic mechanisms.
Review in Molecular medicine (Cambridge, Mass.), 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 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
19 citing papers in PubMed.
- Review
- New structural variations responsible for Charcot-Marie-Tooth disease: The first two largeComputational and structural biotechnology journal · 2021Article
- Article
- Recombinase technology: applications and possibilities.Plant cell reports · 2011Review
- Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines.American journal of human genetics · 2010Article
- KIR genotyping by multiplex PCR-SSP.Methods in molecular biology (Clifton, N.J.) · 2010Article
- Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.Human molecular genetics · 2009Article
- KIR haplotypes defined by segregation analysis in 59 Centre d'Etude Polymorphisme Humain (CEPH) families.Immunogenetics · 2008Article
- Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.Molecular cytogenetics · 2008Article
- A model of segmental duplication formation in Drosophila melanogaster.Genome research · 2007Article
- Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.PloS one · 2007Article
- A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.Human genetics · 2004Article
- Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2.American journal of human genetics · 2002Article
- Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies.American journal of human genetics · 2002Article
- Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae.Molecular and cellular biology · 2001Article
- The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.Genome research · 2001Article
- A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23.American journal of human genetics · 2000Article
- Breaking away from home.American journal of human genetics · 2000Article
- Mouse models of myelin diseases.Brain pathology (Zurich, Switzerland) · 1998Review
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
9513184PMC2230264What 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.