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Familial microtia with meatal atresia in two sibships
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
title
Familial microtia with meatal atresia in two sibships
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
main subject
microtia
1 reference
based on heuristic
inferred from title
genetics
1 reference
stated in
Crossref
DOI
10.1136/JMG.5.4.289
reference URL
https://api.crossref.org/works/10.1136/JMG.5.4.289
retrieved
22 June 2023
author name string
L. C. Ellwood
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
S. T. Winter
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
H. Dar
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
language of work or name
English
0 references
publication date
1 December 1968
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
full work available at URL
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5713641/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5713641/?tool=EBI
file format
HTML
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
https://europepmc.org/articles/PMC1468672
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
https://europepmc.org/articles/PMC1468672?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5713641
retrieved
22 June 2023
https://syndication.highwire.org/content/doi/10.1136/jmg.5.4.289
1 reference
stated in
Crossref
DOI
10.1136/JMG.5.4.289
reference URL
https://api.crossref.org/works/10.1136/JMG.5.4.289
retrieved
22 June 2023
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
volume
5
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
page(s)
289-291
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
cites work
CONGENITAL MEATAL ATRESIA.
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=1468672
retrieved
7 July 2018
PROFOUND CHILDHOOD DEAFNESS.
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=1468672
retrieved
7 July 2018
The first arch 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=1468672
retrieved
7 July 2018
Hereditary cup-shaped ears and the Pierre Robin 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=1468672
retrieved
7 July 2018
Hereditary malformations of the ear in three generations. Marginal pits, pre-auricular appendages, malformations of the auricle and conductive deafness.
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=1468672
retrieved
26 October 2018
Hereditary deafness in family with ear-pits (fistula auris congenita).
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=1468672
retrieved
26 October 2018
Identifiers
DOI
10.1136/JMG.5.4.289
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
5713641
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5713641
retrieved
22 June 2023
PMCID
1468672
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
PubMed ID
5713641
1 reference
stated in
Europe PubMed Central
PubMed ID
5713641
retrieved
3 August 2017
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