(Q67518283)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

title

Structural gene aberrations in mucopolysaccharidosis II (Hunter) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

main subject

mucopolysaccharidosis II

1 reference

chromosomal deletion syndrome

inferred from title

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1352274

17 September 2022

author name string

M. Wehnert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1352274

17 September 2022

J. J. Hopwood

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1352274

17 September 2022

W. Schröder

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1352274

17 September 2022

F. H. Herrmann

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1352274

17 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1352274

17 September 2022

publication date

1 June 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

volume

89

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

14 September 2019

page(s)

430-432

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1352274 AND SRC:MED&resulttype=core&format=json

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

14 September 2019

cites work

1 reference

12 December 2020

Human X chromosome markers and Duchenne muscular dystrophy

1 reference

12 December 2020

A BclI RFLP for DXS296 (VK21) near the fragile X.

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

New distal marker closely linked to the fragile X locus

1 reference

12 December 2020

[Prenatal biochemical diagnosis in genetically-induced metabolic diseases]

1 reference

12 December 2020

Haemophilia B: database of point mutations and short additions and deletions--second edition

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

Characterization of three new deletions at the 5' end of the HPRT structural gene

1 reference

12 December 2020

Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia A.

1 reference

12 December 2020