Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

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The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients

P2860

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P2860

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

Item

http://www.wikidata.org/entity/Q42063901

description

1995 nî lūn-bûn

@nan

1995年の論文

@ja

1995年論文

@yue

1995年論文

@zh-hant

1995年論文

@zh-hk

1995年論文

@zh-mo

1995年論文

@zh-tw

1995年论文

@wuu

1995年论文

@zh

1995年论文

@zh-cn

name

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@en

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@nl

type

Item

label

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@en

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@nl

prefLabel

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@en

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@nl

P1476

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

@en

P2093

Florentin L

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Kekou K

http://www.w3.org/2001/XMLSchema#string

Mavrou A

http://www.w3.org/2001/XMLSchema#string

Metaxotou C

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P2860

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

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

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.

Partial gene duplication in Duchenne and Becker muscular dystrophies.

Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.

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

Detection of novel genetic markers by mismatch analysis.

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

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

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48-51

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scholarly article

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10.1136/JMG.32.1.48

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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1995-01-01T00:00:00Z

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P5875

15300859

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7897627

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P932

1050179

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Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

about

P2860

P2860

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932