(Q35805541)

English

Non-isotopic detection of single strand conformation polymorphism (PCR-SSCP): a rapid and sensitive technique in diagnosis of phenylketonuria

scientific article published on May 1991

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Non-isotopic detection of single strand conformation polymorphism (PCR-SSCP): a rapid and sensitive technique in diagnosis of phenylketonuria (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

phenylketonuria

1 reference

based on heuristic

inferred from title

author name string

Dockhorn-Dworniczak B

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Dworniczak B

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Brömmelkamp L

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Bülles J

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Horst J

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Böcker WW

6

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 May 1991

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

19

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

9

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

2500

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329468

11 July 2018

Phenylketonuria: detection of a frequent haplotype 4 allele mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329468

11 July 2018

Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329468

11 July 2018

Phenylalanine hydroxylase gene: Novel missense mutation in exon 7 causing severe phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329468

11 July 2018

Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles

1 reference

https://pubmed.ncbi.nlm.nih.gov/2041788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/19.9.2500

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

ResearchGate publication ID

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