(Q67513917)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1346924%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

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

1 reference

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14 September 2019

1 reference

8

1 reference

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14 September 2019

author name string

Buxton J

1

1 reference

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14 September 2019

Shelbourne P

2

1 reference

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14 September 2019

Davies J

3

1 reference

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14 September 2019

Jones C

4

1 reference

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14 September 2019

Van Tongeren T

5

1 reference

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14 September 2019

Aslanidis C

6

1 reference

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14 September 2019

de Jong P

7

1 reference

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14 September 2019

Anvret M

9

1 reference

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14 September 2019

Riley B

10

1 reference

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14 September 2019

language of work or name

English

0 references

publication date

1 February 1992

1 reference

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14 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1346924%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

volume

355

1 reference

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14 September 2019

page(s)

547-548

1 reference

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14 September 2019

issue

6360

1 reference

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https://scigraph.springernature.com/pub.10.1038/355547a0

14 September 2019

exact match

0 references

cites work

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

1 reference

7 January 2021

Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids

1 reference

7 January 2021

Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q

1 reference

7 January 2021

CpG-rich islands and the function of DNA methylation

1 reference

7 January 2021

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

1 reference

7 January 2021

Identification of new DNA markers close to the myotonic dystrophy locus

1 reference

7 January 2021

Isolation of cDNA clones using yeast artificial chromosome probes

1 reference

7 January 2021

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

7 January 2021

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

1 reference

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

7 January 2021

Anticipation in myotonic dystrophy: fact or fiction?

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1038/355547A0

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1346924%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference