Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Q24605530)

From Wikidata

Jump to navigation Jump to search

The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

scientific article

Language	Label	Description	Also known as
English	Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

attention deficit hyperactivity disorder

0 references

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Joseph Glessner

6

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

7

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Struan F.A. Grant

16

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Marcella Devoto

18

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

author name string

J Elia

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

X Gai

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

J C Perin

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

E Geiger

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

E Frackelton

9

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

C Kim

10

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

F Lantieri

11

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

B M Muganga

12

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

L Wang

13

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

T Takeda

14

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

E F Rappaport

15

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

W Berrettini

17

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

T H Shaikh

19

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

H Hakonarson

20

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

P S White

21

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

R deBerardinis

8

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

language of work or name

0 references

publication date

23 June 2009

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Molecular Psychiatry

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

15

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

6

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

637-646

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Large recurrent microdeletions associated with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Strong association of de novo copy number mutations with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

MPTP delta, a putative murine homolog of HPTP delta, is expressed in specialized regions of the brain and in the B-cell lineage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

The neuropharmacology of impulsive behaviour

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Strong association of de novo copy number mutations with sporadic schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

The worldwide prevalence of ADHD: a systematic review and metaregression analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Mice lacking metabotropic glutamate receptor 5 show impaired learning and reduced CA1 long-term potentiation (LTP) but normal CA3 LTP

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Increased anxiety-like behavior and enhanced synaptic efficacy in the amygdala of GluR5 knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

Metabotropic glutamate receptor subtype 7 ablation causes deficit in fear response and conditioned taste aversion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

7 April 2017

The Worldwide Prevalence of ADHD: A Systematic Review and Metaregression Analysis

1 reference

https://api.crossref.org/works/10.1038/MP.2009.57

22 April 2017

High-resolution copy-number variation map reflects human olfactory receptor diversity and evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Psychopathology among offspring of parents with schizophrenia: relationship to premorbid impairments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Genetics of attention deficit hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Genomic drift and copy number variation of sensory receptor genes in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

ADHD genetics: 2007 update.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Validity of the World Health Organization Adult ADHD Self-Report Scale (ASRS) Screener in a representative sample of health plan members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Testing for neuropsychological endophenotypes in siblings discordant for attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Developmental and behavioral comorbidities of asthma in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

A faster circular binary segmentation algorithm for the analysis of array CGH data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Hippocampus and amygdala morphology in attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

The relationship between tourette syndrome, attention deficit hyperactivity disorder, and stimulant medication: a critical review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Neuropsychological functioning in people with ADHD across the lifespan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Restless legs syndrome and attention-deficit/hyperactivity disorder: a review of the literature

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Patterns and predictors of attention-deficit/hyperactivity disorder persistence into adulthood: results from the national comorbidity survey replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

The World Health Organization Adult ADHD Self-Report Scale (ASRS): a short screening scale for use in the general population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Genetics of childhood disorders: XXIV. ADHD, part 8: hyperdopaminergic mice as an animal model of ADHD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Pre- and postsynaptic aspects of dopamine-mediated transmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Impaired learning with enhanced hippocampal long-term potentiation in PTPdelta-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Historical development and present status of the schedule for affective disorders and schizophrenia for school-age children (K-SADS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

PicoGreen quantitation of DNA: effective evaluation of samples pre- or post-PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Extensive copy-number variation of the human olfactory receptor gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

27 September 2017

Neuropsychopharmacological mechanisms of stimulant drug action in attention-deficit hyperactivity disorder: a review and integration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

30 May 2018

The prevalence and effects of adult attention deficit/hyperactivity disorder on work performance in a nationally representative sample of workers

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

Cerebellar development and clinical outcome in attention deficit hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

Brain dopamine transporter levels in treatment and drug naïve adults with ADHD.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

Perspective on the genetics of attention deficit/hyperactivity disorder.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

The polymorphisms of protein-tyrosine phosphatase receptor-type delta gene and its association with pediatric asthma in the Taiwanese population

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

Glutamate-stimulated release of norepinephrine in hippocampal slices of animal models of attention-deficit/hyperactivity disorder (spontaneously hypertensive rat) and depression/anxiety-like behaviours (Wistar-Kyoto rat).

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

ADHD symptoms in children with FXS.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

mGluR7 facilitates extinction of aversive memories and controls amygdala plasticity.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

21 January 2018

Medication use in patients with restless legs syndrome compared with a control population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877197

28 November 2018

Young adult outcome of hyperactive children: adaptive functioning in major life activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/19546859

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian Motoneuron Axon Targeting Requires Receptor Protein Tyrosine Phosphatases and

1 reference

https://pubmed.ncbi.nlm.nih.gov/19546859

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene symbol: ATP7B. Disease: Wilson's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene symbol: ATP7B. Disease: Wilson's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene symbol: ATP7B. Disease: Wilson's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene symbol: ATP7B. Disease: Wilson's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene symbol: ATP7B. Disease: Wilson's disease

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.57

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/MP.2009.57

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Dimensions Publication ID

0 references

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19546859%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24605530&oldid=2175201379"