Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33676103)
Watch
English
Menkes disease
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Menkes disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
author name string
Bankier A
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 March 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
volume
32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
page(s)
213-215
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
cites work
A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration
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=1050320
retrieved
21 June 2018
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
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=1050320
retrieved
21 June 2018
Isolation of a partial candidate gene for Menkes disease by positional cloning
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=1050320
retrieved
21 June 2018
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
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=1050320
retrieved
21 June 2018
Recent developments in Menkes disease
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=1050320
retrieved
21 June 2018
Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice
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=1050320
retrieved
21 June 2018
The mottled gene is the mouse homologue of the Menkes disease gene
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=1050320
retrieved
21 June 2018
Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects
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=1050320
retrieved
21 June 2018
Primary defect in copper transport underlies mottled mutants in the mouse
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=1050320
retrieved
21 June 2018
Menkes' kinky hair disease: further definition of the defect in copper transport.
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=1050320
retrieved
21 June 2018
Atypical Menkes steely hair disease.
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=1050320
retrieved
21 June 2018
Kinky hair disease: twenty five years later.
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=1050320
retrieved
21 June 2018
Incidence of Menkes disease
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=1050320
retrieved
21 June 2018
Menkes syndrome in a girl with X-autosome translocation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7783172
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The mild form of Menkes disease: progress report on the original case
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7783172
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.32.3.213
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
PMC publication ID
1050320
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
PubMed publication ID
7783172
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7783172
retrieved
28 July 2017
ResearchGate publication ID
15416369
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit