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Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
title
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
author name string
M G Butler
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
language of work or name
English
0 references
publication date
1 July 1989
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
volume
45
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
page(s)
140-146
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
cites work
The Angelman ("happy puppet") syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Plasma immunoreactive beta-melanocyte stimulating hormone (lipotropin) levels in individuals with Prader-Labhart-Willi syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Is Angelman syndrome an alternate result of del(15)(q11q13)?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Hypopigmentation in the Prader-Willi syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Recurrence risk in the Angelman ("happy puppet") syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683374
retrieved
13 July 2018
Rapid radioimmunoassay for corticotropin in unextracted human plasma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2741944
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2741944
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1683374
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
PubMed publication ID
2741944
1 reference
stated in
Europe PubMed Central
PMC publication ID
1683374
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2741944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 October 2019
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