(Q54199290)

English

Origin of new mutations in Duchenne muscular dystrophy.

scientific article

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scholarly article

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

Origin of new mutations in Duchenne muscular dystrophy. (English)

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

author name string

L Roncuzzi

1

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

A Ferlini

2

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

A Pirozzi

3

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

G Romeo

4

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

publication date

1 December 1986

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

74

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

456-460

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

4

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

https://scigraph.springernature.com/pub.10.1007/bf00280507

0 references

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical trial in Duchenne dystrophy. I. The design of the protocol

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. A population study

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the sex-linked recessive type of muscular dystrophy; a possible sex difference

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878873

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00280507

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

1 reference

Europe PubMed Central

26 May 2018

http://europepmc.org/abstract/MED/2878873

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