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English
Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases
scientific article published on 01 September 1979
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
title
Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
main subject
Prader–Willi syndrome
1 reference
based on heuristic
inferred from title
author
Kim Fleischer Michaelsen
series ordinal
1
object named as
K. F. Michaelsen
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A573673
retrieved
12 July 2022
author name string
C. Lundsteen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A573673
retrieved
12 July 2022
F. J. Hansen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A573673
retrieved
12 July 2022
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
573673
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=573673
retrieved
12 July 2022
publication date
1 September 1979
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
volume
16
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
page(s)
147-150
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
Identifiers
DOI
10.1111/J.1399-0004.1979.TB00983.X
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
PubMed ID
573673
1 reference
stated in
Europe PubMed Central
PubMed ID
573673
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:573673%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 September 2019
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