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English
A case of 9p- syndrome
scientific article published on 01 August 1977
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
title
A case of 9p- syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
author name string
Y Kuroki
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
S Yokota
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
H Nakai
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
Y Yamamoto
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
I Matsui
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
publication date
1 August 1977
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
published in
Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
volume
38
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
page(s)
107-111
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
exact match
https://scigraph.springernature.com/pub.10.1007/bf00295813
0 references
cites work
Comparative behavior of ring chromosomes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A ring 9 chromosome. Repository identification no. GM-166
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mental retardation and congenital malformations associated with a ring chromosome 9.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial deletion of the short arm of the chromosome 9
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A case of annular chromosome 9. Indentification by controlled denaturation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The 9p- syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/903150
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/BF00295813
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
Dimensions Publication ID
1021873004
0 references
PubMed ID
903150
1 reference
stated in
Europe PubMed Central
PubMed ID
903150
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:903150%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 September 2019
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