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A family study of craniosynostosis, with probable recognition of a distinct syndrome.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
title
A family study of craniosynostosis, with probable recognition of a distinct syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
main subject
craniosynostosis
0 references
author name string
C O Carter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
K Till
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
V Fraser
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
R Coffey
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
language of work or name
English
0 references
publication date
1 August 1982
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
page(s)
280-285
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
cites work
Pitfalls of genetic counselling in Pfeiffer'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=1048894
retrieved
21 June 2018
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=1048894
retrieved
21 June 2018
Facial asymmetry and abnormalties of palms and ears: A dominantly inherited developmental 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=1048894
retrieved
21 June 2018
Acrocephalosyndactyly type 3: Chotzen'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=1048894
retrieved
21 June 2018
Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)
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=1048894
retrieved
21 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=1048894
retrieved
21 June 2018
Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly.
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=1048894
retrieved
21 June 2018
A contribution to the clinical picture of acrocephalosyndactylia (Apert'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=1048894
retrieved
30 October 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=1048894
retrieved
30 October 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=1048894
retrieved
30 October 2018
Roentgencephalometric studies of the premature craniofacial synostoses: report of a family with 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=1048894
retrieved
30 October 2018
Genetic perspectives on craniosynostosis and syndromes with 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=1048894
retrieved
30 October 2018
Identifiers
DOI
10.1136/JMG.19.4.280
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PMCID
1048894
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PubMed ID
7120316
1 reference
stated in
Europe PubMed Central
PMCID
1048894
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120316%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
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