(Q39651946)

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22 September 2019

review article

1 reference

title

Molecular analysis of muscular dystrophy (English)

1 reference

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22 September 2019

3

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22 September 2019

Terry J. Smith

4

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22 September 2019

5

S M Forrest

1 reference

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22 September 2019

author name string

K E Davies

1

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22 September 2019

S J Kenwrick

2

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22 September 2019

H R Dorkins

6

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22 September 2019

G S Cross

7

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22 September 2019

S B England

8

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22 September 2019

publication date

1 February 1988

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Journal of Muscle Research & Cell Motility

22 September 2019

published in

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22 September 2019

volume

9

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22 September 2019

issue

1

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22 September 2019

page(s)

1-8

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https://scigraph.springernature.com/pub.10.1007/bf01682143

22 September 2019

exact match

0 references

cites work

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

12 December 2020

Directional cloning of DNA fragments at a large distance from an initial probe: a circularization method

1 reference

12 December 2020

Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis

1 reference

12 December 2020

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms

1 reference

12 December 2020

Origin of new mutations in Duchenne muscular dystrophy.

1 reference

12 December 2020

Is nebulin the defective gene product in Duchenne muscular dystrophy?

1 reference

12 December 2020

Survival in x-chromosomal muscular dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

A linkage study of Emery-Dreifuss muscular dystrophy

1 reference

12 December 2020

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome

1 reference

12 December 2020

Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis

1 reference

12 December 2020

Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.

1 reference

12 December 2020

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients

1 reference

12 December 2020

Clinical features and classification of the muscular dystrophies

1 reference

12 December 2020

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome

1 reference

12 December 2020

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

1 reference

12 December 2020

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome

1 reference

12 December 2020

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male

1 reference

12 December 2020

Conservation of the Duchenne muscular dystrophy gene in mice and humans

1 reference

12 December 2020

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure

1 reference

12 December 2020

Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19

1 reference

12 December 2020

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

12 December 2020

Localisation of genetic markers and orientation of the linkage group on chromosome 19

1 reference

12 December 2020

The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.

1 reference

12 December 2020

A new probe for the diagnosis of myotonic muscular dystrophy

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Protein sequence of DMD gene is related to actin-binding domain of alpha-actinin

1 reference

12 December 2020

Subcellular fractionation of dystrophin to the triads of skeletal muscle

1 reference

12 December 2020

Construction of a general human chromosome jumping library, with application to cystic fibrosis

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

12 December 2020

Long-range restriction map around the Duchenne muscular dystrophy gene

1 reference

12 December 2020

Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families

1 reference

12 December 2020

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

12 December 2020

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

1 reference

12 December 2020

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

12 December 2020

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

12 December 2020

The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.

1 reference

12 December 2020

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

1 reference

12 December 2020

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene

1 reference

12 December 2020

Germline mosaicism and Duchenne muscular dystrophy mutations

1 reference

12 December 2020

Localisation of gene for Becker muscular dystrophy

1 reference

12 December 2020

Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients

1 reference

12 December 2020

Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross

1 reference

12 December 2020

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

12 December 2020

Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.

1 reference

12 December 2020

Familial inheritance of a DXS164 deletion mutation from a heterozygous female

1 reference

12 December 2020

CpG-rich islands and the function of DNA methylation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01682143

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3292577%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference