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Waardenburg syndrome
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title
Waardenburg syndrome
(English)
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author name string
A P Read
series ordinal
1
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V E Newton
series ordinal
2
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language of work or name
English
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publication date
August 1997
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published in
Journal of Medical Genetics
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volume
34
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issue
8
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page(s)
656-65
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cites work
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Homozygosity for Waardenburg syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Waardenburg's syndrome: a comparison of biometric indices used to diagnose lateral displacement of the inner canthi
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Autosomal dominant inheritance of Klein-Waardenburg syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
19 March 2017
Endothelin receptor-mediated signaling in hirschsprung disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Pax3 modulates expression of the c-Met receptor during limb muscle development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
The mutational spectrum in Waardenburg syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Mammalian Pax genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Pax-3 contains domains for transcription activation and transcription inhibition
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Analysis of the mouse Splotch-delayed mutation indicates that the Pax-3 paired domain can influence homeodomain DNA-binding activity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Waardenburg syndrome type II: phenotypic findings and diagnostic criteria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
The human placental alkaline phosphatase gene and related sequences map to chromosome 2 band q37.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Homozygosity in piebald trait
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Mouse and hamster mutants as models for Waardenburg syndromes in humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Pax in development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Heterogeneity in Waardenburg syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Ophthalmological Findings in 34 Patients with Waardenburg Syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
27 September 2017
Deafness as part of an hereditary syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
PAX-genes expression during human embryonic development, a preliminary report.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Pigmentation, pleiotropy, and genetic pathways in humans and mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Hereditary inner-ear abnormalities in animals. Relationships with human abnormalities.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
The Waardenburg syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Hearing loss and Waardenburg's syndrome: implications for genetic counselling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Temporal bone histopathologic findings of Waardenburg's syndrome: a case report
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
30 May 2018
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
29 November 2018
Unraveling the melanocyte.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
29 November 2018
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
29 November 2018
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
29 November 2018
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051028
retrieved
29 November 2018
Possible homozygous Waardenburg syndrome in a fetus with exencephaly
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pigmentary disorders in association with congenital deafness
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Waardenburg's syndrome with bilateral cleft lip
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cleft palate, stapes fixation and oligodontia--a new autosomal recessively inherited syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Tomographic findings of the inner ears of 24 patients with Waardenburg's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Waardenburg's syndrome with fundus and other anomalies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pax-3 is required for the development of limb muscles: a possible role for the migration of dermomyotomal muscle progenitor cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9279758
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.34.8.656
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
475994
OpenCitations bibliographic resource ID
475994
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
475994
PMC publication ID
1051028
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
475994
PubMed publication ID
9279758
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
475994
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