Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences (Q44014712)

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scientific article published in February 1990

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Language	Label	Description	Also known as
English	Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences	scientific article published in February 1990

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scholarly article

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Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

title

Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences (English)

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Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

main subject

Duchenne muscular dystrophy

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inferred from title

author

David N. Cooper

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4

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

author name string

M Hentemann

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1

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

J Reiss

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2

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

M Wagner

series ordinal

3

1 reference

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

publication date

1 February 1990

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stated in

Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

volume

84

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

issue

3

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

page(s)

228-232

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Europe PubMed Central

PubMed publication ID

2303244

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28 November 2017

cites work

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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inferred from PubMed ID database lookup

A deletion hot spot in the Duchenne muscular dystrophy gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular deletions in the Duchenne/Becker muscular dystrophy gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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inferred from PubMed ID database lookup

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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False-positive results and the polymerase chain reaction

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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A catalogue of splice junction sequences

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mut

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

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An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

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Maternal cell contamination in chorionic villus samples assessed by direct preparations and three different culture methods

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited deletion at Duchenne dystrophy locus in normal male

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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Dystrophin. The gene and its product

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

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A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mosaicism and Duchenne muscular dystrophy mutations

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymerase chain reaction: replication errors and reliability of gene diagnosis.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germinal mosaicism in Duchenne muscular dystrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2303244

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12 December 2020

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Identifiers

DOI

10.1007/BF00200564

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

PubMed publication ID

2303244

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2303244

retrieved

28 November 2017

 

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