(Q33668085)

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

6 September 2022

title

Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures (English)

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

6 September 2022

1 reference

1 reference

Horn N

1

1 reference

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

N Horn

series ordinal

1

1 reference

6 September 2022

language of work or name

English

0 references

publication date

1 August 1980

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

Journal of Medical Genetics

6 September 2022

published in

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

6 September 2022

volume

17

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

6 September 2022

issue

4

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

6 September 2022

page(s)

257-261

2 references

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

28 July 2017

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

6 September 2022

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Menkes X linked disease: two clonal cell populations in heterozygotes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

X-chromosome inactivation and developmental patterns in mammals

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Extra-hepatic storage of copper: a male foetus suspected of Menkes' disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Menkes disease: a biochemical abnormality in cultured human fibroblasts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Is Menkes syndrome a copper storage disorder?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Cell culture studies of Menkes kinky hair disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

64Cu metabolism in Menkes and normal cultured skin fibroblasts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048565

Demonstration of the heterozygous state in Hunter's syndrome

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7205900

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Menkes Syndrome: Subcellular Distribution of Copper Determined by an Ultrastructural Histochemical Technique

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7205900

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://api.crossref.org/v1/works/https://doi.org/10.1136/jmg.17.4.257

6 September 2022

1 reference

28 July 2017

1 reference