Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region.

No abstract is available for this paper.

• Publication year

  1993

• Venue

  Human Molecular Genetics

• Publication date

  1993-10-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/HMG/2.10.1667PMID 8268920
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements.

  1993cited by this paper
• Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

  1993cited by this paper
• Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.

  1992cited by this paper
• Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

  1992cited by this paper
• CpG islands as gene markers in the human genome.

  1992cited by this paper
• Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.

  1992cited by this paper
• Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

  1992cited by this paper
• Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach.

  1992cited by this paper
• A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.

  1992cited by this paper
• Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.

  1991cited by this paper
• A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

  1991cited by this paper
• Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.

  1991cited by this paper
• A VNTR isolated by size selection of human DNA fragments detects RFLPs at the extremity of 1p and 4q.

  1991cited by this paper
• Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.

  1990cited by this paper
• Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency.

  1990cited by this paper
• Isolation and characterization of a hypervariable region [D4S163] on chromosome 4.

  1990cited by this paper
• Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.

  1990cited by this paper
• A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storage.

  1990cited by this paper
• Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

  1990cited by this paper
• Isolation of single-copy human genes from a library of yeast artificial chromosome clones.

  1989cited by this paper
• Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139].

  1989cited by this paper
• Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA

  1988cited by this paper
• Clustering of hypervariable minisatellites in the proterminal regions of human autosomes.

  1988cited by this paper
• CpG-rich islands and the function of DNA methylation

  1986cited by this paper
• Genomic sequencing.

  1984cited by this paper
• "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

  1984cited by this paper
• DNA sequencing with chain-terminating inhibitors.

  1977cited by this paper

• DUX4 at 25: how it emerged from “junk DNA” to become the cause of facioscapulohumeral muscular dystrophy

  2025cites this paper
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  2018cites this paper
• Facioscapulohumeral Muscular Dystrophy.

  2017cites this paper
• The Krüppel-like Factor 15 as a Molecular Link between Myogenic Factors and a Chromosome 4q Transcriptional Enhancer Implicated in Facioscapulohumeral Dystrophy*

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  2005cites this paper
• The muscular dystrophies.

  1999cites this paper
• The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements.

  1999cites this paper
• The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.

  1998cites this paper
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  1997cites this paper
• Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).

  1997cites this paper
• Gene table: the muscular dystrophies.

  1997cites this paper
• Neuromuscular disorders: gene location.

  1996cites this paper
• Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.

  1996cites this paper
• The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region.

  1996cites this paper
• Ways of announcing a late-onset, heritable, disabling disease and their psychological consequences.

  1996cites this paper
• Germline mosaicism in 4q35 facioscapulohumeral muscular dystrophy (FSHD1A) occurring predominantly in oogenesis

  1996cites this paper
• Diagnosis in neuromuscular diseases.

  1996cites this paper
• Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.

  1996cites this paper
• Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)

  1995cites this paper
• Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35

  1995cites this paper
• The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

  1995cites this paper
• Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35

  1995cites this paper
• Characterization of a tandemly repeated 3.3‐kb Kpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35

  1995cites this paper
• Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

  1994cites this paper
• Facioscapulohumeral dystrophy: the role of inflammation.

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• Neuromuscular disorders: gene location.

  1994cites this paper
• Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

  1994cites this paper
• 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

  1994cites this paper