Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families (Q33674003)

28 July 2017

title

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families (English)

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Duchenne muscular dystrophy

28 July 2017

main subject

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Bertelson CJ

1

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28 July 2017

Bartley JA

2

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28 July 2017

Monaco AP

3

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28 July 2017

Colletti-Feener C

4

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28 July 2017

Fischbeck K

5

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28 July 2017

Kunkel LM

6

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28 July 2017

language of work or name

English

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publication date

1 December 1986

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

23

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28 July 2017

issue

6

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28 July 2017

page(s)

531-537

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Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus

28 July 2017

cites work

1 reference

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Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

21 June 2018

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

21 June 2018

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Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

21 June 2018

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21 June 2018

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21 June 2018

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Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

21 June 2018

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

21 June 2018

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21 June 2018

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The human met oncogene is related to the tyrosine kinase oncogenes

21 June 2018

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21 June 2018

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

21 June 2018

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Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

21 June 2018

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Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy

21 June 2018

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DNA linkage analysis of X chromosome-linked chronic granulomatous disease

21 June 2018

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A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7.

21 June 2018

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

21 June 2018

1 reference

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Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation

21 June 2018

1 reference

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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

21 June 2018

1 reference

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Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus

21 June 2018

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Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy.

21 June 2018

1 reference

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

21 June 2018

1 reference

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Assay for nanogram quantities of DNA in cellular homogenates

21 June 2018

1 reference

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Molecular Genetics of the Bithorax Complex in Drosophila melanogaster.

21 June 2018

1 reference

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Localization of cystic fibrosis locus to human chromosome 7cen–q22

30 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Inherited interstitial del(Xp) with minimal clinical consequences: with a note on the location of genes controlling phenotypic features

1 reference

12 December 2020

Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy

1 reference

12 December 2020

A closely linked genetic marker for cystic fibrosis

1 reference

12 December 2020

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

12 December 2020

Identifiers

0 references

1 reference

28 July 2017

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