(Q24676840)

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Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

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title

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene (English)

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author name string

J Mossman

series ordinal

1

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S Blunt

series ordinal

2

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R Stephens

series ordinal

3

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E E Jones

series ordinal

4

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M Pembrey

series ordinal

5

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language of work or name

English

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publication date

November 1983

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published in

Archives of Disease in Childhood

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volume

58

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page(s)

911-5

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issue

11

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cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628393

retrieved

28 September 2017

Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628393

retrieved

28 September 2017

The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1628393

retrieved

28 September 2017

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6418082

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6418082

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in Hunter syndrome

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Crossref

reference URL

https://api.crossref.org/works/10.1136%2FADC.58.11.911

retrieved

7 January 2021

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Identifiers

DOI

10.1136/ADC.58.11.911

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Fatcat ID

release_yqwqpised5a7raobhrfclp6qhy

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Fatcat

reference URL

https://api.fatcat.wiki/v0/release/yqwqpised5a7raobhrfclp6qhy

retrieved

24 November 2022

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ResearchGate publication ID

16778384

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(Q24676840)

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

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