(Q57747773)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12891378%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population (English)

1 reference

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6 November 2019

4

1 reference

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6 November 2019

Adamo Pio d'Adamo

8

1 reference

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6 November 2019

author name string

Sylvain R Rivard

1

1 reference

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6 November 2019

Carmela Lanzara

2

1 reference

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6 November 2019

Doria Grimard

3

1 reference

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6 November 2019

Hervey Simard

5

1 reference

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6 November 2019

Romina Ficarella

6

1 reference

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6 November 2019

Raynald Simard

7

1 reference

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6 November 2019

Claude Férec

9

1 reference

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6 November 2019

Clara Camaschella

10

1 reference

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6 November 2019

Cathrine Mura

11

1 reference

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6 November 2019

Antonella Roetto

12

1 reference

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6 November 2019

Lucien Bechner

14

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6 November 2019

Paolo Gasparini

15

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6 November 2019

Marc De Braekeleer

13

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6 November 2019

publication date

1 August 2003

1 reference

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European Journal of Human Genetics

6 November 2019

published in

1 reference

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6 November 2019

volume

11

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6 November 2019

page(s)

585-589

1 reference

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6 November 2019

issue

8

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201009

6 November 2019

exact match

0 references

cites work

Natural history of juvenile haemochromatosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Juvenile hemochromatosis locus maps to chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Hemochromatosis and pyruvate kinase deficiency. Report of a case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): a study of inbreeding

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

A prevalence and fertility study of haemochromatosis in Saguenay-Lac-Saint-Jean

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Juvenile haemochromatosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201009

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12891378%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference