(Q67521824)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

Gene diagnosis and carrier detection in Hunter syndrome by the iduronate-2-sulphatase cDNA probe (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author

Charles Phillip Morris

4

1 reference

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14 September 2019

6

J J Hopwood

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author name string

A Gal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

M Beck

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

A C Sewell

3

1 reference

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14 September 2019

E Schwinger

5

1 reference

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14 September 2019

publication date

1 January 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357230%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

14 September 2019

published in

1 reference

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14 September 2019

volume

15

1 reference

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14 September 2019

issue

3

1 reference

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14 September 2019

page(s)

342-346

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf02435972

14 September 2019

exact match

0 references

cites work

Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA

1 reference

12 December 2020

Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type II

1 reference

12 December 2020

The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome)

1 reference

12 December 2020

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

12 December 2020

Heterozygote detection in Hunter syndrome

1 reference

12 December 2020

Genetic mapping of new RFLPs at Xq27–q28

1 reference

12 December 2020

Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020