Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy (Q35196020)

7 August 2017

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy (English)

1 reference

7 August 2017

1 reference

5

E P Hoffman

1 reference

7 August 2017

L S Schwartz

1

1 reference

7 August 2017

J Tarleton

series ordinal

2

1 reference

7 August 2017

B Popovich

series ordinal

3

1 reference

7 August 2017

W K Seltzer

series ordinal

4

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 October 1992

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

51

1 reference

7 August 2017

4

1 reference

7 August 2017

721-729

1 reference

Prediction of carrier status in Duchenne dystrophy by creatine kinase measurement.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

A simple salting out procedure for extracting DNA from human nucleated cells

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

A polymorphic CACA repeat in the 3' untranslated region of dystrophin.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

13 July 2018

Dystrophin and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682805

Identification of a nondeletion defect in alpha-thalassemia

13 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1415217

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1415217

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1682805

1 reference

7 August 2017

1 reference