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English
Rett syndrome--a review and discussion of syndrome delineation and syndrome definition.
scientific article published on January 1987
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
Rett syndrome--a review and discussion of syndrome delineation and syndrome definition
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
main subject
Rett syndrome
0 references
author name string
J M Opitz
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
S O Lewin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
publication date
1 January 1987
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
published in
Brain and Development
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
page(s)
445-450
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
cites work
[Mutation and phenocopy in mammals and man; their theoretical and practical importance for genetics and eugenics]
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of ornithine transcarbamylase deficiency with Rett syndrome manifestations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome revisited: a patient with biotin dependency.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the genetics of Rett syndrome: analysis of family and pedigree data.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage analysis of the Rett syndrome using human chromosomal specific probes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome. A commonly overlooked progressive encephalopathy in girls
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Rett syndrome: genetics and the future
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the genetics of the Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980061-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0387-7604(87)80061-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
PubMed publication ID
3324794
1 reference
stated in
Europe PubMed Central
PubMed publication ID
3324794
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3324794%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
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