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English
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?
scientific article published in May 1994
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
title
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
main subject
deafness
1 reference
based on heuristic
inferred from title
author
Martin J van den Bent
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author name string
Linssen WH
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Brunner HG
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Poels PJ
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
publication date
1 May 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
volume
51
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
page(s)
81-82
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
cites work
Hereditary sensory neuropathy with deafness: a familial multisystem atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FAJMG.1320510117
retrieved
21 January 2018
Identifiers
DOI
10.1002/AJMG.1320510117
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
PubMed publication ID
8030674
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8030674
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8030674%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
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