ArticleAmerican journal of human genetics1992
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).
Article in American journal of human genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed, 35 citations in OpenAlex.
- International Union of Basic and Clinical Pharmacology. LXXV. Nomenclature, classification, and pharmacology of G protein-coupled melatonin receptors.Pharmacological reviews · 2010Article
- New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?European journal of human genetics : EJHG · 2010Article
- Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level.European journal of human genetics : EJHG · 2009Article
- Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.Journal of medical genetics · 1998Article
- Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.Journal of medical genetics · 1996Article
- Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique.Human genetics · 1994Article
- Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).Human genetics · 1994Article
- The incidence of mini- and micro-satellite repetitive DNA in the canine genome.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 1994Article
- The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1994Article
- A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).American journal of human genetics · 1993Article
- The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.Human genetics · 1993Article
- Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.American journal of human genetics · 1992Article
- The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).American journal of human genetics · 1992Article
- Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.Mammalian genome : official journal of the International Mammalian Genome Society · 1992Article
- Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.Mammalian genome : official journal of the International Mammalian Genome Society · 1992Article
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
Abstract
We have used a combination of classical RFLPs and PCR-based polymorphisms including CA repeats and single-strand conformation polymorphisms to generate a fine-structure genetic map of the distal long arm of chromosome 4q. This map is now genetically linked to the pre-existing anchor map of 4pter-4q31 and generates, for the first time, a complete linkage map of this chromosome. The map consists of 32 anchor loci placed with odds of greater than 1,000:1. The high-resolution map in the cytogenetic region surrounding 4q35 provides the order 4cen-D4S171-F11-D4S187-D4S163-D4S139-4q ter. When we used somatic cell hybrids from a t(X;4)(p21;q35) translocation, these five markers fell into three groups consistent with the genetic map-D4S171 and F11 in 4pter-4q35, D4S163 and D4S139 in 4q35-4qter, and D4S187 as a junction fragment between these two regions. These markers are in tight linkage to the gene for facioscapulo-humeral muscular dystrophy (FSHD) mapped to this region by several collaborating investigators and provide a framework for further detailed analysis of this region.
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1642243PMC1682692W2336222324What 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.