(Q33669942)

28 July 2017

A clinical and genetic study of Hunter's syndrome. 1. Heterogeneity (English)

1 reference

28 July 2017

Young ID

1

1 reference

28 July 2017

Harper PS

series ordinal

2

1 reference

28 July 2017

Archer IM

series ordinal

3

1 reference

28 July 2017

Newcombe RG

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 December 1982

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

19

1 reference

28 July 2017

6

1 reference

28 July 2017

401-407

1 reference

A sex-linked variant of gargoylism

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

The systemic mucopolysaccharidoses.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Limitations of metachromasia as a diagnostic aid in pediatrics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Hurler's syndrome. A genetic study in cell culture

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Mild and severe Hunter syndrome (MPS II) within the same sibships

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Detection of hunter heterozygotes by enzymatic analysis of hair roots

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Clinical heterogeneity in mucopolysaccharidosis. II. Evidence for epistasis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048950

Clinical and probable genetic heterogeneity within mucopolysaccharidosis. II. Report of a family with a mild form

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6818347

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic heterogeneity and allelic variation in the mucopolysaccharidoses. Introduction

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6818347

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6818347

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

0 references

1 reference

28 July 2017

1 reference