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Ring chromosome 13 syndrome
scientific article published on March 1, 1975
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
title
Ring chromosome 13 syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
main subject
human chromosomes 13-15
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
multiple abnormalities
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
chromosome abnormality
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
genetics
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
author name string
K. Fried
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
M. Rosenblatt
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
G. Mundel
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
R. Krikler
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1139790
retrieved
25 August 2022
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
1139790
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1139790
retrieved
25 August 2022
publication date
1 March 1975
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
full work available at URL
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1975.tb00320.x
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1975.tb00320.x/fullpdf
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
volume
7
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
page(s)
203-208
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
cites work
The 13q-deletion syndrome
series ordinal
1
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Multiple congenital abnormalities associated with ring chromosome
series ordinal
2
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Mental retardation and congenital malformations associated with a ring chromosome 6
series ordinal
4
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Chromosome studies in 5,049 consecutive newborn children
series ordinal
5
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
The 13q- deletion syndrome
series ordinal
7
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Multiple congenital anomalies associated with a ring-D chromosome
series ordinal
10
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Retinoblastoma and D-chromosome deletions
series ordinal
13
1 reference
stated in
Crossref
DOI
10.1111/J.1399-0004.1975.TB00320.X
reference URL
https://api.crossref.org/works/10.1111/J.1399-0004.1975.TB00320.X
retrieved
12 October 2023
Identifiers
DOI
10.1111/J.1399-0004.1975.TB00320.X
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
1139790
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1139790
retrieved
25 August 2022
PubMed ID
1139790
1 reference
stated in
Europe PubMed Central
PubMed ID
1139790
retrieved
14 October 2017
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