Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy (Q33597984)

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

Bodrug SE

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Roberson JR

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Weiss L

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Ray PN

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Worton RG

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Van Dyke DL

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 July 1990

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

426-432

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Balanced structural changes involving the human X: Effect on sexual phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Chapter 7: Isolation of Mutants of Cultured Mammalian Cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Muscular dystrophy in girls with X;autosome translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

A cDNA clone from the Duchenne/Becker muscular dystrophy gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

A practical metaphase marker of the inactive X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

21 June 2018

Unexpected relationships between four large deletions in the human beta-globin gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

30 October 2018

Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017179

30 October 2018

X-autosome translocations: cytogenetic characteristics and their consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-range restriction map around the Duchenne muscular dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular heterogeneity of translocations associated with muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic analysis of two human reciprocal X-autosome translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of mutations of the retinoblastoma gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2395160

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.27.7.426

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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