Hereditary tyrosinemia in a French Canadian isolate (Q35231846)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Hereditary tyrosinemia in a French Canadian isolate	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

title

Hereditary tyrosinemia in a French Canadian isolate (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

author name string

C. Laberge

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5763606

retrieved

26 June 2023

language of work or name

English

0 references

publication date

1 January 1969

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5763606/pdf/?tool=EBI

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5763606

retrieved

26 June 2023

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5763606/?tool=EBI

file format

HTML

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5763606

retrieved

26 June 2023

https://europepmc.org/articles/PMC1706398

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5763606

retrieved

26 June 2023

https://europepmc.org/articles/PMC1706398?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5763606

retrieved

26 June 2023

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

volume

21

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

page(s)

36-45

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

cites work

Segregation of the Ellis-van Creveld Syndrome as Analyzed by the First Appearance Method

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

TYROSINEMIA.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

PYRUVATE KINASE DEFICIENT HEMOLYTIC ANEMIA IN AN AMISH ISOLATE

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

DWARFISM IN THE AMISH I. THE ELLIS-VAN CREVELD SYNDROME

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

Clinical and biochemical study of three patients with tyrosyluria

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

Experience with 37 infants with tyrosinemia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

Hereditary tyrosinemia and tyrosyluria: clinical report of four patients

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

Tyrosinosis. A study of 6 cases

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

A simple method of estimating the segregation ratio under complete ascertainment

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

The enzymatic deficiency in tyrosinemia.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

13 July 2018

HUNTINGTON'S CHOREA IN FRENCH CANADIANS. PRELIMINARY STUDY

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706398

retrieved

26 September 2018

Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5763606

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FAMILIAL HEPATIC CIRRHOSIS IN INFANCY

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5763606

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TYROSINOSIS

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5763606

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1706398

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

PubMed publication ID

5763606

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5763606

retrieved

7 August 2017

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35231846&oldid=1980102339"