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English
Saethre-Chotzen syndrome
scientific article published on May 1994
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Saethre-Chotzen syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
author name string
Reardon W
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
Winter RM
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
language of work or name
English
0 references
publication date
1 May 1994
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
volume
31
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
page(s)
393-396
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
issue
5
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
cites work
Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.
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=1049872
retrieved
22 September 2017
An unusual form of familial acrocephalosyndactyly.
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=1049872
retrieved
22 September 2017
A family study of craniosynostosis, with probable recognition of a distinct 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=1049872
retrieved
22 September 2017
Auralcephalosyndactyly: a new hereditary craniosynostosis 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=1049872
retrieved
22 September 2017
Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen 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=1049872
retrieved
22 September 2017
The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p
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=1049872
retrieved
22 September 2017
Sutural biology and the correlates of craniosynostosis
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=1049872
retrieved
25 September 2017
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.
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=1049872
retrieved
15 June 2018
Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.
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=1049872
retrieved
15 June 2018
The Saethre-Chotzen 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=1049872
retrieved
15 June 2018
Pfeiffer syndrome: report of a family 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=1049872
retrieved
15 June 2018
The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one 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=1049872
retrieved
19 August 2018
Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases
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=1049872
retrieved
19 August 2018
Is loss of band 7p21 really critical for manifestation of craniosynostosis in 7p-?
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=1049872
retrieved
19 August 2018
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22
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=1049872
retrieved
19 August 2018
Acrocephalopolysyndactyly, type Noack, in a large kindred
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=1049872
retrieved
19 August 2018
Identifiers
DOI
10.1136/JMG.31.5.393
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
PMCID
1049872
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
PubMed ID
8064818
1 reference
stated in
Europe PubMed Central
PMCID
1049872
retrieved
22 September 2017
ResearchGate publication ID
270153078
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