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The 13q- deletion syndrome
scientific article published on September 1, 1971
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
title
The 13q- deletion syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
main subject
human chromosomes 13-15
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
chromosome abnormality
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
genetics
1 reference
stated in
Crossref
DOI
10.1136/JMG.8.3.351
reference URL
https://api.crossref.org/works/10.1136/JMG.8.3.351
retrieved
15 December 2023
author name string
E. Grace
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
J. Drennan
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
D. Colver
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
R. R. Gordon
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
language of work or name
English
0 references
publication date
1 September 1971
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
full work available at URL
https://jmg.bmj.com/content/jmedgenet/8/3/351.full.pdf
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097142/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5097142/?tool=EBI
file format
HTML
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
https://europepmc.org/articles/PMC1469176
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
https://europepmc.org/articles/PMC1469176?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
5097142
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5097142
retrieved
15 December 2023
https://syndication.highwire.org/content/doi/10.1136/jmg.8.3.351
1 reference
stated in
Crossref
DOI
10.1136/JMG.8.3.351
reference URL
https://api.crossref.org/works/10.1136/JMG.8.3.351
retrieved
15 December 2023
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
volume
8
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
page(s)
351-357
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
cites work
The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes
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=1469176
retrieved
7 July 2018
CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.
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=1469176
retrieved
7 July 2018
Absent thumbs with a ring D2 chromosome: a new deletion 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=1469176
retrieved
7 July 2018
A human ring D chromosome associated with multiple congenital 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=1469176
retrieved
7 July 2018
A ring D chromosome and anomalous inheritance of haptoglobin type
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=1469176
retrieved
7 July 2018
The 13q-deletion 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=1469176
retrieved
7 July 2018
Chromosome abnormalities in two cases with bilateral radial element defects
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=1469176
retrieved
7 July 2018
Ring chromosomes in two infants with congenital malformations
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=1469176
retrieved
7 July 2018
Retinoblastoma and deletion D (14) 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=1469176
retrieved
7 July 2018
Multiple congenital anomalies associated with a ring-D chromosome
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=1469176
retrieved
7 July 2018
The Dr phenotype: a study of threee cases with a ring D chromosome
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=1469176
retrieved
7 July 2018
Ring D1 chromosome and multiple malformations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ring D chromosome: a second case associated with anomalous haptoglobin inheritance
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A case of D ring chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Multiple congenital abnormalities associated with ring chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial deletion of the long arm of a group D (13-15) chromosome :Dq-
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097142
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.8.3.351
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PMCID
1469176
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PubMed ID
5097142
1 reference
stated in
Europe PubMed Central
PMCID
1469176
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097142%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
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