(Q41822557)

English

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

scientific article published on November 1990

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

author name string

A H Beggs

1

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

M Koenig

2

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

F M Boyce

3

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

L M Kunkel

4

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

publication date

1 November 1990

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

86

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

45-48

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

describes a project that uses

polymerase chain reaction

1 reference

based on heuristic

inferred from title

Dystrophin abnormalities in Duchenne/Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved diagnosis of Becker muscular dystrophy by dystrophin testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved diagnosis of Duchenne/Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-reactive protein in Duchenne muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial gene duplication in Duchenne and Becker muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2253937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00205170

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 October 2017

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