(Q35221857)

7 August 2017

1 reference

title

Myotonic dystrophy: another case of too many repeats? (English)

1 reference

7 August 2017

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1301924

10 September 2022

2

Johnson K

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1301924

10 September 2022

author name string

Shelbourne P

series ordinal

1

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=1301924

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

3

1 reference

7 August 2017

page(s)

183-189

1 reference

Proposed genetic basis of Huntington's disease

7 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

A new probe for the diagnosis of myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Identification of new DNA markers close to the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Radiation-reduced hybrids for the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Mspl RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Anticipation in myotonic dystrophy: fact or fiction?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

A primary map of ten DNA markers and two serological markers for human chromosome 19

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Assignment of the structural gene for the third component of human complement to chromosome 19.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010302

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380010302

1 reference

7 August 2017

1 reference