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English
A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
title
A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
main subject
albinism
1 reference
based on heuristic
inferred from title
author name string
TIETZ W
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
language of work or name
English
0 references
publication date
1 September 1963
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
volume
15
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
page(s)
259-264
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
cites work
A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital 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=1932384
retrieved
7 April 2017
Deafness as part of an hereditary 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=1932384
retrieved
30 May 2018
Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/13985019
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A New Hereditary Syndrome – Sex-linked Deaf-mutism Associated with Total Albinism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/13985019
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1932384
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
PubMed ID
13985019
1 reference
stated in
Europe PubMed Central
PMCID
1932384
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13985019%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 December 2019
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