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Prader-Willi syndrome.
scientific article published in February 1989
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Prader-Willi syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
author name string
Cassidy SB
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
Ledbetter DH
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
publication date
1 February 1989
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
published in
Neurologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
volume
7
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
page(s)
37-54
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
cites work
Pathology of muscular hypotonia in the Prader-Willi syndrome. Light and electron microscopic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recurrence risk in Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prader-Willi syndrome. Variable severity and recurrence risk
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of proximal 15q without Prader-Willi syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adults with Prader-Willi syndrome: a survey of 232 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cytogenetic controversy in the Prader-Labhart-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linear growth response to exogenous growth hormone in Prader-Willi syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial Prader-Willi syndrome with apparently normal chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is Angelman syndrome an alternate result of del(15)(q11q13)?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paternal hydrocarbon exposure in Prader-Willi syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Emotional symptoms in Prader-Willi syndrome adolescents.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High Resolution of Human Chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characteristics of abnormal food-intake patterns in children with Prader-Willi syndrome and study of effects of naloxone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(18)30827-2
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
PubMed ID
2646521
1 reference
stated in
Europe PubMed Central
PubMed ID
2646521
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 October 2019
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