(Q24538685)

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Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype

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scholarly article

1 reference

Europe PubMed Central

5 July 2017

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Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype (English)

1 reference

Europe PubMed Central

5 July 2017

12

object named as

Morgan K

1 reference

Europe PubMed Central

5 July 2017

Jocelyne Mercier

9

object named as

Mercier J

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Europe PubMed Central

5 July 2017

author name string

Bétard C

1

1 reference

Europe PubMed Central

5 July 2017

Rasquin-Weber A

2

1 reference

Europe PubMed Central

5 July 2017

Brewer C

3

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Europe PubMed Central

5 July 2017

Drouin E

4

1 reference

Europe PubMed Central

5 July 2017

Clark S

5

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Europe PubMed Central

5 July 2017

Verner A

6

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Europe PubMed Central

5 July 2017

Darmond-Zwaig C

7

1 reference

Europe PubMed Central

5 July 2017

Fortin J

8

1 reference

Europe PubMed Central

5 July 2017

Chagnon P

10

1 reference

Europe PubMed Central

5 July 2017

Fujiwara TM

11

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Europe PubMed Central

5 July 2017

Richter A

13

1 reference

Europe PubMed Central

5 July 2017

Hudson TJ

14

1 reference

Europe PubMed Central

5 July 2017

Mitchell GA

15

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Europe PubMed Central

5 July 2017

language of work or name

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publication date

11 May 2000

1 reference

Europe PubMed Central

5 July 2017

American Journal of Human Genetics

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Europe PubMed Central

5 July 2017

67

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Europe PubMed Central

5 July 2017

1

1 reference

Europe PubMed Central

5 July 2017

222-228

1 reference

Europe PubMed Central

5 July 2017

Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Carrier detection in Sandhoff disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

An allele of COL9A2 associated with intervertebral disc disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Byler disease. Fatal familial intrahepatic cholestasis in an Amish kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

24 March 2017

Faster sequential genetic linkage computations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

7 April 2017

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

7 April 2017

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

27 September 2017

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

27 September 2017

The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

27 September 2017

Familial intrahepatic cholestatic jaundice in infancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

27 September 2017

Hereditary polymorphic light eruption of American Indians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

27 September 2017

Autosomal recessive microcephaly and micromelia in Cree Indians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

30 May 2018

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

30 May 2018

Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

29 November 2018

Automatic selection of loop breakers for genetic linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

29 November 2018

Faster linkage analysis computations for pedigrees with loops or unused alleles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

29 November 2018

Avoiding recomputation in linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

29 November 2018

Leukoencephalopathy among native Indian infants in northern Quebec and Manitoba

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287080

29 November 2018

Familial jaundice caused by intrahepatic cholestasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive familial cholestatic cirrhosis and bile acid metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal familial cholestatic syndrome in Greenland Eskimo children

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsyndromic paucity of interlobular bile ducts: clinical and laboratory findings of 10 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive familial intrahepatic cholestasis among the Arab population in Israel

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of isolated inbred human populations for identification of disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide scanning for type 2 diabetes susceptibility in Canadian Oji-Cree, using 190 microsatellite markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/10820129

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://api.crossref.org/works/10.1086%2F302993

7 January 2021

based on heuristic

inferred from DOI database lookup

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Europe PubMed Central

5 July 2017

1 reference

Europe PubMed Central

5 July 2017

1 reference

Europe PubMed Central

5 July 2017

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