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English
Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1.
scientific article published on 6 June 2001
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
case report
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title
Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
otopalatodigital syndrome type 2
0 references
otopalatodigital syndrome
1 reference
based on heuristic
inferred from title
author
Andrew Oliver Mungo Wilkie
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Stephen Robertson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
Walsh S
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Oldridge M
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Gunn T
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Becroft D
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
language of work or name
English
0 references
publication date
6 June 2001
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
69
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
223-227
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Are Melnick-Needles syndrome and oto-palato-digital syndrome type II allelic? Observations in a four-generation kindred
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=1226038
retrieved
28 July 2018
A comprehensive genetic map of the human genome based on 5,264 microsatellites
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226038
retrieved
28 July 2018
A compositional map of human chromosome band Xq28
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=1226038
retrieved
28 July 2018
Faster sequential genetic linkage computations
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=1226038
retrieved
28 July 2018
The oto-palato-digital syndrome, proposed type II.
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=1226038
retrieved
28 July 2018
The oto-palato-digital syndrome. A new symptom-complex consisting of deafness, dwarfism, cleft palate, characteristic facies, and a generalized bone dysplasia
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=1226038
retrieved
28 July 2018
Oto-palato-digital syndrome: comparison of clinical and radiographic manifestations in males and females
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=1226038
retrieved
28 July 2018
The oto-palato-digital (OPD) syndrome in females
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=1226038
retrieved
28 July 2018
Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization
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=1226038
retrieved
28 July 2018
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28
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=1226038
retrieved
28 July 2018
Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28)
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=1226038
retrieved
28 July 2018
Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
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=1226038
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28 July 2018
A familial syndrome of cranial, facial, oral and limb anomalies
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226038
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28 July 2018
Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasia
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226038
retrieved
29 October 2018
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
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=1226038
retrieved
29 October 2018
Familial skewed X inactivation and X-linked mutations: unbalanced X inactivation is a powerful means to ascertain X-linked genes that affect cell proliferation
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=1226038
retrieved
29 October 2018
Avoiding recomputation in linkage analysis.
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=1226038
retrieved
29 October 2018
Easy calculations of lod scores and genetic risks on small computers
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=1226038
retrieved
29 October 2018
Generalized skeletal dysplasia with multiple anomalies. A note on Pyle'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=1226038
retrieved
29 October 2018
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11398100
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Age- and tissue-specific variation of X chromosome inactivation ratios in normal women
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11398100
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1086/321280
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PMCID
1226038
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed ID
11398100
1 reference
stated in
Europe PubMed Central
PMCID
1226038
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11398100%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
ResearchGate publication ID
11941693
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