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The Coffin-Lowry syndrome
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
The Coffin-Lowry syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
main subject
Coffin-Lowry syndrome
1 reference
based on heuristic
inferred from title
author name string
Young ID
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 May 1988
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
volume
25
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
page(s)
344-348
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
cites work
Brief clinical report: early recognition of the Coffin-Lowry 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=1050463
retrieved
21 June 2018
The Coffin-Lowry syndrome. A study of two new index patients and their families.
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=1050463
retrieved
21 June 2018
A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.
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=1050463
retrieved
21 June 2018
Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's 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=1050463
retrieved
21 June 2018
Coffin-Lowry syndrome and schizophrenia: a family report.
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=1050463
retrieved
21 June 2018
The Coffin-Lowry syndrome: a facio digital mental retardation syndrome: a case report
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=1050463
retrieved
21 June 2018
The Coffin-Lowry syndrome: an inherited faciodigital mental retardation 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=1050463
retrieved
21 June 2018
The Coffin 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=1050463
retrieved
21 June 2018
The Coffin-Lowry syndrome. Experience from four centres.
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=1050463
retrieved
30 October 2018
[The coffin, Siris, Wegienka syndrome]
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The syndrome of Coffin, Siris and Wegienka: report of a case
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Coffin-Lowry syndrome in an Afro-American family
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Orodental findings and genetic disorders
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3290491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.25.5.344
0 references
PMCID
1050463
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
PubMed ID
3290491
1 reference
stated in
Europe PubMed Central
PubMed ID
3290491
retrieved
28 July 2017
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