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English
The detection of carriers in hereditary myoclonic epilepsy
scientific article published on 01 October 1960
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
title
The detection of carriers in hereditary myoclonic epilepsy
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
main subject
myoclonic epilepsy
1 reference
based on heuristic
inferred from title
author name string
M B SARLIN
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
H W KLOEPFER
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
W A MICKLE
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
R G HEATH
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
publication date
1 October 1960
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
published in
Acta geneticae medicae et gemellologiae
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
page(s)
466-471
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
cites work
The heredity of epilepsy as told by relatives and twins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300018199
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300018199
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonus epilepsy as a symptom of diffuse neuronal disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS1120962300018199
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S1120962300018199
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
PubMed ID
13746547
1 reference
stated in
Europe PubMed Central
PubMed ID
13746547
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13746547%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 December 2019
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