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English
A syndrome of ocular abnormalities, calcification of cartilage, and failure to thrive
scientific article published on 01 October 1968
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
title
A syndrome of ocular abnormalities, calcification of cartilage, and failure to thrive
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
author name string
H H Punnett
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
J A Kirkpatrick
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
language of work or name
English
0 references
publication date
1 October 1968
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
published in
The Journal of Pediatrics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
volume
73
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
page(s)
602-606
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
cites work
Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980277-X
retrieved
7 January 2021
A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2868%2980277-X
retrieved
7 January 2021
Identifiers
DOI
10.1016/S0022-3476(68)80277-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
PubMed publication ID
4234212
1 reference
stated in
Europe PubMed Central
PubMed publication ID
4234212
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4234212%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 September 2019
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