Applications of capillary electrophoresis in DNA mutation analysis of genetic disorders (Q40727315)

23 September 2017

Applications of capillary electrophoresis in DNA mutation analysis of genetic disorders (English)

1 reference

23 September 2017

0 references

Le H

1

1 reference

23 September 2017

Fung D

series ordinal

2

1 reference

23 September 2017

Trent RJ

series ordinal

3

1 reference

23 September 2017

language of work or name

English

0 references

publication date

1 October 1997

1 reference

Journal of Clinical Pathology

23 September 2017

1 reference

23 September 2017

50

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23 September 2017

5

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23 September 2017

261-265

1 reference

Screening and identification of familial defective apolipoprotein B-100 in clinical samples by capillary gel electrophoresis

23 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

Slowly but surely towards better scanning for mutations

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

Replaceable polymers in DNA sequencing by capillary electrophoresis

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

Semi-automated detection of the factor V mutation by allele specific amplification and capillary electrophoresis.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379643

Molecular analysis of common aldolase B alleles for hereditary fructose intolerance in North Americans

19 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9497917

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fluorescence-based polymerase chain reaction-single-strand conformation polymorphism analysis of p53 gene by capillary electrophoresis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9497917

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/MP.50.5.261

1 reference

23 September 2017

1 reference

23 September 2017

1 reference