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English
Roberts syndrome: clinical and cytogenetic aspects.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
title
Roberts syndrome: clinical and cytogenetic aspects
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
main subject
Roberts syndrome
1 reference
based on heuristic
inferred from title
author name string
N P Mann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
J Fitzsimmons
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
E Fitzsimmons
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
P Cooke
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
language of work or name
English
0 references
publication date
1 April 1982
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
page(s)
116-119
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
cites work
Familial holoprosencephaly with endocrine dysgenesis.
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=1048840
retrieved
21 June 2018
The SC phocomelia and the Roberts syndrome: nosologic aspects
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=1048840
retrieved
21 June 2018
Roberts's syndrome and clonidine
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=1048840
retrieved
21 June 2018
Roberts' syndrome.I. Cytological evidence for a disturbance in chromatid pairing
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=1048840
retrieved
21 June 2018
The Roberts 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=1048840
retrieved
30 October 2018
A sibship with the pseudothalidomide syndrome and an association with Rh incompatibility
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7077622
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic counselling: the one-in-four risk of a rare disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7077622
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.19.2.116
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
PMC publication ID
1048840
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
PubMed publication ID
7077622
1 reference
stated in
Europe PubMed Central
PMC publication ID
1048840
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7077622%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 October 2019
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