(Q66703225)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

title

Fluorimetric assay for prenatal detection of Hurler and Scheie homozygotes or heterozygotes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

author name string

J. L. Stirling

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A87574

14 November 2022

D. Robinson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A87574

14 November 2022

A. H. Fensom

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A87574

14 November 2022

P. F. Benson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A87574

14 November 2022

J. E. Baker

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A87574

14 November 2022

language of work or name

English

0 references

publication date

1 January 1978

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

21 January 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=87574

full work available at URL

14 November 2022

https://api.elsevier.com/content/article/PII:S0140673678904415?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(78)90441-5

https://api.elsevier.com/content/article/PII:S0140673678904415?httpAccept=text/plain

14 November 2022

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(78)90441-5

14 November 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

volume

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

issue

8056

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

page(s)

147

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.

23 August 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Fibroblast phosphodiesterase deficiency in Niemann-Pick disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

I-cell disease: biochemical studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Tay-Sachs Disease: Prenatal Diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Hurler's syndrome, an -L-iduronidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

A method for alpha-L-iduronidase assay

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Infantile Hypoglycaemia due to Inherited Deficiency of Glycogen Synthetase in Liver

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Hepatic glycogen synthetase deficiency. Definition of syndrome from metabolic and enzyme studies on a 9-year-old girl

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Blood cell glycogen synthetase activities in hepatic glycogen synthetase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2878%2990441-5

7 January 2021

Protein measurement with the Folin phenol reagent

8

1 reference

https://api.crossref.org/works/10.1016/S0140-6736(78)90441-5

14 November 2022

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:87574%20AND%20SRC:MED&resulttype=core&format=json

23 August 2019

1 reference