(Q60641503)

English

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis

scientific article published on 01 October 1990

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scholarly article

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26 September 2019

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis (English)

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Europe PubMed Central

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26 September 2019

Duchenne muscular dystrophy

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5

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26 September 2019

author name string

D O Robinson

1

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26 September 2019

Y Boyd

2

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26 September 2019

D Cockburn

3

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26 September 2019

M N Collinson

4

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26 September 2019

P A Jacobs

6

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26 September 2019

publication date

1 October 1990

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26 September 2019

Genetics Research

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56

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26 September 2019

2-3

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26 September 2019

135-140

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26 September 2019

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect

1 reference

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7 January 2021

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Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

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Meiosis in man.

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical features and classification of the muscular dystrophies

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Complex chromosome rearrangements. Report of a new case and literature review

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Parental origin of de novo chromosome rearrangements

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensation

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene.

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the committee on the genetic constitution of the X chromosome

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Duchenne muscular dystrophy in a girl with an (X;15) translocation

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1017%2FS0016672300035217

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1017/S0016672300035217

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2272503%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2272503%20AND%20SRC:MED&resulttype=core&format=json

26 September 2019

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