(Q35911447)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

title

The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference

W E KNOX

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

E C MESSINGER

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

language of work or name

English

0 references

publication date

1 March 1958

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

13 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

page(s)

53-60

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

The amino acid content of the blood and urine in Wilson's disease

13 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931862

A case of phenylketonuria with borderline intelligence.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931862

The excretion of amino acids by the human; a quantitative study with ion-exchange chromatography

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931862

The hydroxylation of phenylalanine and antipyrine in phenylpyruvic oligophrenia.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931862

Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931862

Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies

24 September 2018

1 reference

12 December 2020

Pathogenetic problems in phenylketonuria

1 reference

12 December 2020

Detection of the heterozygous carriers of phenylketonuria

1 reference

12 December 2020

Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of Phenylketonuria

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13520699%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference