Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q35957032)
Watch
English
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
title
Screening, counselling and treatment of hereditary metabolic disease; a survey of resources in Canada
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
main subject
Canada
0 references
metabolic disease
1 reference
based on heuristic
inferred from title
author
Charles R. Scriver
series ordinal
3
object named as
Scriver CR
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
retrieved
11 August 2017
author name string
Haworth JC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
Miller JR
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
Scriver CR
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
language of work or name
English
0 references
publication date
1 November 1974
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
published in
Canadian Medical Association Journal
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
volume
111
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
issue
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
page(s)
1147-50, 1153
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
cites work
Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.
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=1955842
retrieved
2 October 2017
Medical research policy for Canada. I. The evolution and convolution of policy, politics and dollars
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=1955842
retrieved
2 October 2017
The frequency of genetic disease and congenital malformation among patients in a pediatric hospital
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=1955842
retrieved
2 October 2017
The incidence of genetic disease in a University hospital population
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=1955842
retrieved
2 October 2017
On the application of knowledge to the patient with genetic 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=1955842
retrieved
2 October 2017
The genetic component in child mortality
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=1955842
retrieved
24 September 2018
Thyroxine (T4) determination by radioimmunological method in dried blood eluate: new diagnostic method of neonatal hypothyroidism?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/4429943
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1955842
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
PubMed publication ID
4429943
1 reference
stated in
Europe PubMed Central
PMC publication ID
1955842
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4429943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
27 September 2019
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