(Q35548147)

8 August 2017

title

Evidence for genetic anticipation in nodal osteoarthritis (English)

1 reference

8 August 2017

1 reference

1

Wright GD

1 reference

8 August 2017

5

Doherty M

1 reference

8 August 2017

Regan M

2

1 reference

8 August 2017

Deighton CM

series ordinal

3

1 reference

8 August 2017

Wallis G

series ordinal

4

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 September 1998

1 reference

Annals of the Rheumatic Diseases

8 August 2017

published in

1 reference

8 August 2017

volume

57

1 reference

8 August 2017

issue

9

1 reference

8 August 2017

page(s)

524-526

1 reference

HEBERDEN'S NODES: THE MECHANISM OF INHERITANCE IN HYPERTROPHIC ARTHRITIS OF THE FINGERS.

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

GENETIC FACTORS IN GENERALIZED OSTEO-ARTHROSIS

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Association of two loci on chromosome 2q with nodal osteoarthritis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Preliminary evidence for genetic anticipation in Crohn's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Genetic influences on osteoarthritis in women: a twin study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Anticipation in bipolar affective disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Allelic instability in mitosis: a unified model for dominant disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Discordance for autoimmunity in monozygotic twins. Are "identical" twins really identical?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Evidence for anticipation in schizophrenia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Triplet repeat genes raise questions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Does genetic anticipation occur in familial rheumatoid arthritis?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Huntington disease in Georgia: age at onset

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

Anticipation in myotonic dystrophy: new light on an old problem

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1752739

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

27 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9849310

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/ARD.57.9.524

1 reference

release_25tlcomigfhvpkl6kzk4pa2kkm

8 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/25tlcomigfhvpkl6kzk4pa2kkm

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

1752739

1 reference

8 August 2017

1 reference