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English
Genotype and phenotype in Angelman syndrome caused by paternal UPD 15
scientific article published on 01 June 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
title
Genotype and phenotype in Angelman syndrome caused by paternal UPD 15
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
main subject
Angelman syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author name string
C Prasad
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
J Wagstaff
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 June 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
number of pages
2
1 reference
based on heuristic
inferred from page(s)
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
70
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
328-329
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
cites work
Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Uniparental paternal disomy in Angelman's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Angelman syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970613%2970%3A3%3C328%3A%3AAID-AJMG21%3E3.0.CO%3B2-M
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-8628(19970613)70:3<328::AID-AJMG21>3.0.CO;2-M
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
9188675
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9188675
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9188675%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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