Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q69890442)
Watch
English
Molecular genetics of PKU
scientific article published on 01 January 1986
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
title
Molecular genetics of PKU
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
main subject
molecular genetics
1 reference
based on heuristic
inferred from title
author name string
F Güttler
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
S L Woo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
publication date
1 January 1986
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
published in
Journal of Inherited Metabolic Disease
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
volume
9 Suppl 1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
page(s)
58-68
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
exact match
https://scigraph.springernature.com/pub.10.1007/bf01800859
0 references
cites work
Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Prenatal diagnosis of classical phenylketonuria by gene mapping
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Detection of phenylalanine hydroxylase messenger RNA in liver biopsy samples from patients with phenylketonuria
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Gene transfer and expression of human phenylalanine hydroxylase
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/2878116
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/BF01800859
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Dimensions Publication ID
1040327230
0 references
PubMed publication ID
2878116
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2878116
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878116%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 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