(Q35221861)

7 August 2017

title

Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene (English)

1 reference

7 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1301934

10 September 2022

author name string

Baldrich K

1

1 reference

7 August 2017

Baldrich M

2

1 reference

7 August 2017

Monaco AP

3

1 reference

7 August 2017

Müller CR

4

1 reference

7 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1301934

10 September 2022

publication date

1 January 1992

1 reference

7 August 2017

1 reference

7 August 2017

volume

1

1 reference

7 August 2017

issue

4

1 reference

7 August 2017

page(s)

280-287

1 reference

Effects of poly[d(pGpT).d(pApC)] and poly[d(pCpG).d(pCpG)] repeats on homologous recombination in somatic cells

7 August 2017

cites work

1 reference

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Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

The rate of spontaneous mutation of a human gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Genetics of Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Sequences of junction fragments in the deletion-prone region of the dystrophin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Base sequence studies of 300 nucleotide renatured repeated human DNA clones

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Structural intermediates of deletion mutagenesis: a role for palindromic DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Sequence-specific cleavage of double helical DNA by triple helix formation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

A 24-base-pair DNA sequence from the MAT locus stimulates intergenic recombination in yeast

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Are intron-encoded specific endonucleases responsible for nonhomologous recombination?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

N segment insertion and region-directed somatic hypermutation in a kappa gene of a t(2;8) chromosomal translocation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

The t(14;18) chromosome translocations involved in B-cell neoplasms result from mistakes in VDJ joining

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Hypervariable minisatellites: recombinators or innocent bystanders?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

The structure and evolution of the human beta-globin gene family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Nucleotide sequence preference at rat liver and wheat germ type 1 DNA topoisomerase breakage sites in duplex SV40 DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Unexpected relationships between four large deletions in the human beta-globin gene cluster

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Recombination at the human alpha-globin gene cluster: sequence features and topological constraints

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Germline mosaicism and Duchenne muscular dystrophy mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010403

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380010403

1 reference

7 August 2017

1 reference