(Q67894054)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

title

First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

First-trimester diagnosis of hunter syndrome: Very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus (English)

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

2 December 2022

author name string

A. Cooper

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1820774

2 December 2022

M. Thornley

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1820774

2 December 2022

J. E. Wraith

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1820774

2 December 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=1820774

2 December 2022

publication date

1 September 1991

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

18 September 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fpd.1970110911

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

https://onlinelibrary.wiley.com/doi/full/10.1002/pd.1970110911

2 December 2022

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

2 December 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

page(s)

731-735

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase

18 September 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Full expression of Hunter's disease in a female with an X-chromosome deletion leading to non-random inactivation

2 December 2022

2

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Intrauterine diagnosis of the hurler and hunter syndromes

2 December 2022

3

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Chorionic villus sampling: diagnostic uses and limitations of enzyme assays

2 December 2022

4

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Prenatal monitoring for the Hunter syndrome: The heterozygous female fetus

2 December 2022

7

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

First trimester diagnosis of Hunter syndrome on chorionic villi

2 December 2022

8

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Iduronate sulfatase in amniotic fluid: An aid in the prenatal diagnosis of the Hunter syndrome

2 December 2022

9

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Protein measurement with the Folin phenol reagent

2 December 2022

10

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Feasibility of first trimester prenatal diagnosis of Hunter syndrome

2 December 2022

11

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Gene action in the X-chromosome of the mouse (Mus musculus L.)

2 December 2022

12

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans

2 December 2022

14

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

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

2 December 2022

15

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Prenatal diagnosis of Hunter syndrome using chorionic villi.

2 December 2022

16

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase

2 December 2022

17

1 reference

https://api.crossref.org/works/10.1002/PD.1970110911

2 December 2022

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1820774%20AND%20SRC:MED&resulttype=core&format=json

18 September 2019

1 reference