(Q36627217)

English

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

scientific article published on January 1984

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

15 August 2017

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

1 reference

Europe PubMed Central

15 August 2017

muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

C Verellen-Dumoulin

1

1 reference

Europe PubMed Central

15 August 2017

M Freund

2

1 reference

Europe PubMed Central

15 August 2017

R De Meyer

3

1 reference

Europe PubMed Central

15 August 2017

C Laterre

4

1 reference

Europe PubMed Central

15 August 2017

J Frédéric

5

1 reference

Europe PubMed Central

15 August 2017

M W Thompson

6

1 reference

Europe PubMed Central

15 August 2017

V D Markovic

7

1 reference

Europe PubMed Central

15 August 2017

R G Worton

8

1 reference

Europe PubMed Central

15 August 2017

publication date

1 January 1984

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

67

1 reference

Europe PubMed Central

15 August 2017

115-119

1 reference

Europe PubMed Central

15 August 2017

1

1 reference

Europe PubMed Central

15 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00270570

0 references

Abnormalities of the electrocardiogram in hereditary myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual type of benign x-linked muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved technique for selective silver staining of nucleolar organizer regions in human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The vectorcardiogram in Duchenne's progressive muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late replicating bands of human chromosomes demonstrated by fluorochrome and Giemsa staining

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Frank Vectorcardiogram and the Electrocardiogram in Duchenne Progressive Muscular Dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication pattern of the X chromosomes in three X/autosomal translocations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne's muscular dystrophy: the electrocardiogram in female relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical studies in benign (Becker type) X-linked muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Giemsa method for the differential staining of sister chromatids

1 reference

https://pubmed.ncbi.nlm.nih.gov/6745920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00270570

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

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=Q36627217&oldid=1641669109"