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Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
title
Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
main subject
Prader–Willi syndrome
1 reference
based on heuristic
inferred from title
author name string
T Reed
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
M G Butler
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
publication date
1 April 1984
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
volume
25
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
page(s)
341-346
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
cites work
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=5490795
retrieved
28 July 2018
Dermatoglyphics in medicine--problems and use in suspected chromosome abnormalities
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=5490795
retrieved
28 July 2018
Parental origin of chromosome 15 deletion in 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=5490795
retrieved
28 July 2018
Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation)
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=5490795
retrieved
28 July 2018
Hypotonia, mental retardation, obesity, and cryptorchidism associated with dwarfism and diabetes in children
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=5490795
retrieved
28 July 2018
Dermatoglyphic analyses of 24 individuals with 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=5490795
retrieved
29 October 2018
Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6713710
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dermatoglyphics in Prader-Willi syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6713710
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The Prader-Willi syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6713710
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1111/J.1399-0004.1984.TB02001.X
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PMC publication ID
5490795
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PubMed publication ID
6713710
1 reference
stated in
Europe PubMed Central
PMC publication ID
5490795
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6713710%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
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