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An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
An autosomal dominant syndrome of renal and anogenital malformations with syndactyly
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
main subject
syndactyly
0 references
author
Andrew Green
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
author name string
R N Sandford
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
B C Davison
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
language of work or name
English
0 references
publication date
1 July 1996
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
33
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
594-596
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
cites work
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.
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=1050669
retrieved
28 July 2018
Anorectal malformation: familial aspects and associated anomalies
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=1050669
retrieved
28 July 2018
A new family with the Townes-Brocks syndrome
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=1050669
retrieved
28 July 2018
Townes-Brocks syndrome. Report of a case and review of the literature
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=1050669
retrieved
28 July 2018
The Townes-Brocks syndrome
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=1050669
retrieved
28 July 2018
Familial caudal dysgenesis: evidence for a major dominant gene
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=1050669
retrieved
28 July 2018
Sacrococcygeal dysgenesis association
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=1050669
retrieved
28 July 2018
Triad of anorectal, sacral, and presacral anomalies
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=1050669
retrieved
30 October 2018
Dominantly inherited renal adysplasia
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=1050669
retrieved
30 October 2018
A familial syndrome of renal, genital, and middle ear anomalies
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818947
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary urogenital adysplasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818947
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The VATER association. Analysis of 46 patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818947
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Vaginal atresia (von Mayer-Rokitansky-Küster or MRK anomaly) in hereditary renal adysplasia (HRA)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818947
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ano-rectal abnormalities as a congenital familial incidence
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818947
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.33.7.594
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PMC publication ID
1050669
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PubMed publication ID
8818947
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818947%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
ResearchGate publication ID
14386280
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