(Q33668093)

28 July 2017

Menkes X linked disease: two clonal cell populations in heterozygotes (English)

1 reference

28 July 2017

Horn N

1

1 reference

28 July 2017

Mooy P

series ordinal

2

1 reference

28 July 2017

McGuire VM

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 August 1980

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

17

1 reference

28 July 2017

262-266

1 reference

28 July 2017

4

1 reference

Protein measurement with the Folin phenol reagent

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

Sex chromatin and gene action in the mammalian X-chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

Menkes X linked disease: heterozygous phenotype in uncloned fibroblast cultures

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

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=1048566

Menkes kinky hair syndrome in a black infant.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

Menkes' kinky hair disease: further definition of the defect in copper transport.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

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=1048566

Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048566

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=1048566

Pili torti as marker for carriers 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=1048566

Detection of proximal-vein thrombosis by Doppler ultrasound flow-detection method

21 June 2018

1 reference

12 December 2020

Copper metabolism in Menkes disease

1 reference

12 December 2020

Prenatal diagnosis of Menkes' disease

1 reference

12 December 2020

Menkes syndrome: subcellular distribution of copper determined by an ultrastructural histochemical technique

1 reference

12 December 2020

Identifiers

PMCID

1048566

1 reference

28 July 2017

1 reference