(Q33585609)

28 July 2017

title

Tissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuria (English)

1 reference

28 July 2017

1 reference

Bittles AH

1

1 reference

28 July 2017

Carson NA

series ordinal

2

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 June 1973

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

10

1 reference

28 July 2017

issue

2

1 reference

28 July 2017

page(s)

120-121

1 reference

Protein measurement with the Folin phenol reagent

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

The identification of homocystine in the urine

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012999

Studies of the mechanism of pyridoxine-responsive homocystinuria

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4714577

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/4714577

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1012999

1 reference

28 July 2017

1 reference