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English
Silver's syndrome: report of a case with chromosomal and dermatoglyphic study
scientific article published on 01 March 1967
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
title
Silver's syndrome: report of a case with chromosomal and dermatoglyphic study
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
author name string
P E Ferrier
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
S A Ferrier
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
language of work or name
English
0 references
publication date
1 March 1967
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
published in
The Journal of Pediatrics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
volume
70
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
page(s)
438-440
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
cites work
Syndrome of congenital hemihypertrophy and elevated urinary gonadotropins; occurrence in a seven-year-old boy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980146-X
retrieved
7 January 2021
ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980146-X
retrieved
7 January 2021
A Girl with Triploid Cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980146-X
retrieved
7 January 2021
CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0022-3476%2867%2980146-X
retrieved
7 January 2021
Identifiers
DOI
10.1016/S0022-3476(67)80146-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
PubMed publication ID
6018399
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6018399
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6018399%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
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