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English
PTEN mutations and proteus syndrome
scientific article published in December 2001
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
title
PTEN mutations and proteus syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
main subject
Proteus syndrome
1 reference
based on heuristic
inferred from title
author name string
C Eng
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
H Thiele
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
X P Zhou
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
R J Gorlin
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
R C Hennekam
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
R M Winter
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
publication date
1 December 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
volume
358
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
issue
9298
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
page(s)
2079-2080
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
cites work
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2907110-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2907110-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in GLI3 in postaxial polydactyly type A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2907110-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2907110-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Conversion of diploidy to haploidy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2801%2907110-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(01)07110-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
PubMed publication ID
11755639
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11755639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11755639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 May 2020
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