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English
Growing interest in Turner syndrome
scientific article published on 01 May 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
title
Growing interest in Turner syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
main subject
Turner syndrome
1 reference
based on heuristic
inferred from title
author
Andrew R. Zinn
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 May 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
16
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
3-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0597-3
0 references
cites work
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Whither Down syndrome critical regions?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0597-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0597-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
9140381
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9140381
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9140381%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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