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English
Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: case report with autopsy
scientific article published on 01 March 1980
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
title
Partial deletion of chromosome 2 mimicking a phenotype of trisomy 18: case report with autopsy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
main subject
Past photo
1 reference
based on heuristic
litr
partial deletion of chromosome 2
0 references
case report
1 reference
based on heuristic
litr
phenotype
1 reference
based on heuristic
litr
author name string
T S McConnell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
M Kornfeld
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
G McClellan
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
J Aase
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
publication date
1 March 1980
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
published in
Human Pathology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
volume
11
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
page(s)
202-205
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
cites work
Mapping Human Autosomes: Assignment of the MN Locus to a Specific Segment in the Long Arm of Chromosome No. 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2880%2980146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2880%2980146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2880%2980146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0046-8177%2880%2980146-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0046-8177(80)80146-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PubMed publication ID
7399508
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7399508
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7399508%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
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