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English
Molecular basis of mild hyperphenylalaninaemia in Poland.
scientific article published in December 1997
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
Molecular basis of mild hyperphenylalaninaemia in Poland
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
Poland
1 reference
based on heuristic
inferred from title
author
Jerzy Bal
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
C Zekanowski
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
M Nowacka
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
B Cabalska
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
language of work or name
English
0 references
publication date
1 December 1997
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
34
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
1035-1036
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Molecular basis of non-PKU hyperphenylalaninaemia in Spain: prevalence of A403V, a mutation with high residual activity
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=1051162
retrieved
21 June 2018
Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood
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=1051162
retrieved
21 June 2018
Molecular basis for nonphenylketonuria hyperphenylalaninemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9429153
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Frequencies of the most common mutations responsible for phenylketonuria in Poland
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9429153
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemias
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9429153
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Relation between phenylalanine hydroxylase genotypes and phenotypic parameters of diagnosis and treatment of hyperphenylalaninaemic disorders. German Collaborative Study of PKU
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9429153
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.34.12.1035
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PMC publication ID
1051162
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
9429153
1 reference
stated in
Europe PubMed Central
PMC publication ID
1051162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9429153%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
ResearchGate publication ID
13801579
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