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English
The Marshall and Stickler syndromes: objective rejection of lumping.
scientific article published on February 1984
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
title
The Marshall and Stickler syndromes: objective rejection of lumping
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
author name string
S Aymé
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
M Preus
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
language of work or name
English
0 references
publication date
1 February 1984
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
volume
21
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
page(s)
34-38
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
cites work
Retinal detachment in median cleft-face 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=1049203
retrieved
6 June 2018
Marshall/Stickler 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=1049203
retrieved
6 June 2018
Hereditary vitreoretinal degeneration, cleft lip and palate, deafness, and skeletal dysplasia.
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=1049203
retrieved
6 June 2018
Formal analysis of dysmorphism: objective methods of syndrome definition.
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=1049203
retrieved
6 June 2018
The numerical versus intuitive approach to syndrome nosology.
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=1049203
retrieved
6 June 2018
The Marshall syndrome: report of a new family
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=1049203
retrieved
6 June 2018
Hyalo-retinopathy in the clefting 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=1049203
retrieved
6 June 2018
Stickler's syndrome (hereditary progressive arthro-ophthalmopathy).
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=1049203
retrieved
6 June 2018
Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait
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=1049203
retrieved
6 June 2018
Inherited hyaloideoretinopathy and skeletal dysplasia
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=1049203
retrieved
6 June 2018
Generalized osseous abnormalities in the Marshall 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=1049203
retrieved
6 June 2018
The Stickler syndrome (hereditary arthroophthalmopathy)
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=1049203
retrieved
6 June 2018
Vitreoretinal Degeneration as a Sign of Generalized Connective Tissue Diseases
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=1049203
retrieved
6 June 2018
Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect.
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=1049203
retrieved
18 August 2018
A case of heriditary arthro-ophthalmopathy: Stickler's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6694183
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Letter: The demise of the Marshall syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6694183
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Stickler's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6694183
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary progressive arthro-ophthalmopathy of Stickler
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6694183
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.21.1.34
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PMC publication ID
1049203
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PubMed publication ID
6694183
1 reference
stated in
Europe PubMed Central
PMC publication ID
1049203
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6694183%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
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