(Q35200364)

7 August 2017

title

Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information (English)

1 reference

7 August 2017

7

Morton NE

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7 August 2017

1

Lalouel JM

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7 August 2017

Le Mignon L

2

1 reference

7 August 2017

Simon M

3

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7 August 2017

Fauchet R

4

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7 August 2017

Bourel M

5

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7 August 2017

Rao DC

6

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7 August 2017

language of work or name

English

0 references

publication date

1 July 1985

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

37

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7 August 2017

issue

4

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7 August 2017

page(s)

700-718

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Resolution of linkage for irregular phenotype systems

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=1684619

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

The genetics of hemochromatosis.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Genetic mapping: chromosomes 6-22.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

A unified model for complex segregation analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

A General Model for the Genetic Analysis of Pedigree Data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

An immunoradiometric assay for ferritin in the serum of normal subjects and patients with iron deficiency and iron overload

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Analysis of family resemblance. 3. Complex segregation of quantitative traits

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Serum ferritin concentration and iron stores in normal subjects

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Skewness in commingled distributions

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Heredity of idiopathic haemochromatosis: a study of 106 families

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Analysis of family resemblance. IV. Operational characteristics of segregation analysis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Genetic linkage between hereditary hemochromatosis and HLA

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Hereditary hemochromatosis. Phenotypic expression of the disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Bivariate analyses of cholesterol and triglyceride levels in families in which probands have type IIb lipoprotein phenotype

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Influence of Food Iron Absorption on the Plasma Iron Level in Idiopathic Hemochromatosis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Genetic analysis of von Willebrand's disease in two large pedigrees: a multivariate approach

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684619

Idiopathic hemochromatosis, an iron storage disease. A. Iron metabolism in hemochromatosis

26 September 2018

1 reference

12 December 2020

Serotyping for homotransplantation. 18. Refinement of microdroplet lymphocyte cytotoxicity test

1 reference

12 December 2020

Measurement of liver-iron concentration in needle-biopsy specimens

1 reference

12 December 2020

An HLA-All association with the hemochromatosis allele?

1 reference

12 December 2020

The determination of iron in blood plasma or serum

1 reference

12 December 2020

The determination of the total iron-binding capacity of serum

1 reference

12 December 2020

Letter: Idiopathic hemochromatosis associated with HL-A 3 tissular antigen

1 reference

12 December 2020

The role of iron in the regulation of hepatic transferrin synthesis

1 reference

12 December 2020

Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing

1 reference

12 December 2020

A simple scheme for the analysis of HLA linkages in pedigrees

1 reference

12 December 2020

A familial study in idiopathic hemochromatosis

1 reference

12 December 2020

Identifiers

PMC publication ID

1684619

1 reference

7 August 2017

1 reference