(Q36423793)

English

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

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Duchenne muscular dystrophy

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Margaret A. Pericak-Vance

8

object named as

Pericak-Vance MA

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

9

object named as

Roses AD

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

author name string

Bertelson CJ

2

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Middlesworth W

3

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Colletti CA

4

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Aldridge J

5

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Fischbeck KH

6

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Bartlett R

7

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Kunkel LM

10

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

language of work or name

0 references

publication date

1 August 1985

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

316

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

6031

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

842-845

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

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/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Lambda Charon vectors (Ch32, 33, 34 and 35) adapted for DNA cloning in recombination-deficient hosts

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Lambda replacement vectors carrying polylinker sequences

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

SERUM ENZYME STUDIES IN MUSCLE DISEASE. III. SERUM CREATINE KINASE ACTIVITY IN RELATIVES OF PATIENTS WITH THE DUCHENNE TYPE OF MUSCULAR DYSTROPHY.

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci

1 reference

https://api.crossref.org/works/10.1038%2F316842A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/316842A0

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36423793&oldid=2269657621"