(Q40398851)

20 September 2017

'Broad-range' DGGE for single-step mutation scanning of entire genes: application to human phenylalanine hydroxylase gene (English)

1 reference

20 September 2017

Guldberg P

1

1 reference

PMC publication ID

307896

20 September 2017

Güttler F

series ordinal

2

1 reference

20 September 2017

1 March 1994

1 reference

20 September 2017

2

1 reference

inferred from page(s)

published in

Nucleic Acids Research

1 reference

20 September 2017

22

1 reference

20 September 2017

5

1 reference

20 September 2017

880-881

1 reference

Current methods of mutation detection

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307896

Detection and localization of single base changes by denaturing gradient gel electrophoresis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307896

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307896

Molecular analysis of phenylketonuria in Denmark: 99% of the mutations detected by denaturing gradient gel electrophoresis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307896

Detection of single base substitutions in total genomic DNA

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8139930

12 December 2020

inferred from PubMed ID database lookup

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8139930

12 December 2020

inferred from PubMed ID database lookup

Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8139930

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/NAR/22.5.880

1 reference

20 September 2017

1 reference

PMC publication ID

307896

20 September 2017

PubMed publication ID

8139930

1 reference

PMC publication ID

307896