(Q33595010)

28 July 2017

title

Rapid and efficient PCR/StyI test for identification of common mutation R408W in phenylketonuria patients (English)

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28 July 2017

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Ivaschenko T

1

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28 July 2017

Baranov VS

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 February 1993

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

30

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28 July 2017

issue

2

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28 July 2017

page(s)

153-154

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Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase

28 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016274

Application of natural and amplification created restriction sites for the diagnosis of PKU mutations

14 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016274

Restriction enzymes and their isoschizomers.

14 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016274

Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction

14 July 2018

1 reference

12 December 2020

Rapid diagnosis of the phenylketonuria haplotype 2 mutation by DNA amplification and MnlI digestion

1 reference

12 December 2020

Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R.

1 reference

12 December 2020

Polymerase chain reaction amplification from dried blood spots on Guthrie cards

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.30.2.153

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28 July 2017

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28 July 2017

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