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English
Fraser syndrome presenting as bilateral renal agenesis in three sibs
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
title
Fraser syndrome presenting as bilateral renal agenesis in three sibs
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
main subject
Fraser syndrome
1 reference
based on heuristic
inferred from title
renal agenesis
1 reference
based on heuristic
inferred from title
author name string
Burn J
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
Marwood RP
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 October 1982
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
volume
19
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
page(s)
360-361
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
cites work
Cryptophthalmos in Two Families from Bahia, Brazil
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048921
retrieved
21 June 2018
A family study of renal agenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048921
retrieved
21 June 2018
A familial syndrome of renal, genital, and middle ear anomalies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7143389
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Malformative Syndrome with Cryptophthalmos
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7143389
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1048921
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
PubMed ID
7143389
1 reference
stated in
Europe PubMed Central
PubMed ID
7143389
retrieved
28 July 2017
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