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English
Dominant piebald trait (white forelock and leukoderma) with neurological impairment.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
title
Dominant piebald trait (white forelock and leukoderma) with neurological impairment
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
author name string
Telfer MA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
Sugar M
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
Jaeger EA
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
Mulcahy J
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
language of work or name
English
0 references
publication date
1 July 1971
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
volume
23
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
page(s)
383-389
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 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=1706704
retrieved
26 September 2018
Partial albinism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097904
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pigmentary disorders in association with congenital deafness
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097904
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial white skin spotting (piebaldness) ("partial albinism") with white forelock
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097904
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Partial albinism and deaf-mutism due to a recessive sex-linked gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/5097904
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1706704
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PubMed publication ID
5097904
1 reference
stated in
Europe PubMed Central
PMC publication ID
1706704
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5097904%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
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