Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73187090)
Watch
English
Interstitial 4p deletion in a child with an Angelman syndrome-like phenotype
scientific article published on 01 September 1999
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
title
Interstitial 4p deletion in a child with an Angelman syndrome-like phenotype
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
main subject
phenotype
1 reference
based on heuristic
inferred from title
author
A. Micheil Innes
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
author name string
A E Chudley
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
N L Carson
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
A J Dawson
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
publication date
1 September 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
56
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
238-241
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
cites work
Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Proximal 4p-deletion: phenotype differs from classical 4p-syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syndrome of proximal interstitial deletion 4p15
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and clinical study of 61 Angelman syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angelman syndrome: clinical profile
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angelman syndrome assessed by neurological and molecular cytogenetic investigations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560311.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1399-0004.1999.560311.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
10563486
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10563486
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563486%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
