(Q35231846)

7 August 2017

title

Hereditary tyrosinemia in a French Canadian isolate (English)

1 reference

7 August 2017

C. Laberge

1

1 reference

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

26 June 2023

language of work or name

English

0 references

publication date

1 January 1969

1 reference

full work available at URL

7 August 2017

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

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

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

26 June 2023

1 reference

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

https://europepmc.org/articles/PMC1706398

26 June 2023

1 reference

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

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

26 June 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

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

American Journal of Human Genetics

26 June 2023

published in

1 reference

7 August 2017

volume

21

1 reference

7 August 2017

issue

1

1 reference

7 August 2017

page(s)

36-45

1 reference

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

7 August 2017

cites work

1 reference

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

13 July 2018

1 reference

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

PYRUVATE KINASE DEFICIENT HEMOLYTIC ANEMIA IN AN AMISH ISOLATE

13 July 2018

1 reference

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

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

13 July 2018

1 reference

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

The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis

13 July 2018

1 reference

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

Clinical and biochemical study of three patients with tyrosyluria

13 July 2018

1 reference

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

Experience with 37 infants with tyrosinemia

13 July 2018

1 reference

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

Hereditary tyrosinemia and tyrosyluria: clinical report of four patients

13 July 2018

1 reference

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

Tyrosinosis. A study of 6 cases

13 July 2018

1 reference

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

A simple method of estimating the segregation ratio under complete ascertainment

13 July 2018

1 reference

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

The enzymatic deficiency in tyrosinemia.

13 July 2018

1 reference

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

HUNTINGTON'S CHOREA IN FRENCH CANADIANS. PRELIMINARY STUDY

13 July 2018

1 reference

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

Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate

26 September 2018

1 reference

PubMed

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

FAMILIAL HEPATIC CIRRHOSIS IN INFANCY

1 reference

PubMed

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1706398

1 reference

7 August 2017

1 reference