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An unusual form of familial acrocephalosyndactyly.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
title
An unusual form of familial acrocephalosyndactyly
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
author name string
I D Young
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
P S Harper
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%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
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%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
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
volume
19
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
page(s)
286-288
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
cites work
Variable expression in Pfeiffer 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=1048895
retrieved
21 June 2018
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=1048895
retrieved
21 June 2018
Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating
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=1048895
retrieved
21 June 2018
Pfeiffer syndrome. An unusual type of acrocephalosyndactyly with broad thumbs and great toes
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=1048895
retrieved
30 October 2018
Familial acrocephalosyndactyly (Pfeiffer 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=1048895
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=1048895
retrieved
30 October 2018
On the classification of the acrocephalosyndactyly syndromes
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=1048895
retrieved
30 October 2018
Identifiers
DOI
10.1136/JMG.19.4.286
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PMCID
1048895
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
PubMed ID
7120317
1 reference
stated in
Europe PubMed Central
PMCID
1048895
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7120317%20AND%20SRC:MED&resulttype=core&format=json
retrieved
11 October 2019
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