HFEGenotype Frequencies in Consecutive Reference Laboratory Specimens: Comparisons among Referral Sources and Association with Initial Diagnosis-Reference-Cited by-同舟云学术

HFEGenotype Frequencies in Consecutive Reference Laboratory Specimens: Comparisons among Referral Sources and Association with Initial Diagnosis

Published:2001-12 Issue:4 Volume:5 Page:299-306
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Acton Ronald T.¹,Barton James C.²

Affiliation:

1. Immunogenetics Program, Departments of Microbiology, Medicine, and Epidemiology, University of Alabama at Birmingham, AL 35294

2. Immunogenetics Program, Department of Medicine, University of Alabama at Birmingham, AL 35294 and Southern Iron Disorders Center, Birmingham, AL 35209

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/109065701753617426

Reference51 articles.

1. Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis

2. Role of genetic testing and liver biopsy in the diagnosis of hemochromatosis

3. HFE Genotype in Patients with Hemochromatosis and Other Liver Diseases

4. Transferrin Saturation Phenotype andHFEGenotype Screening for Hemochromatosis and Primary Iron Overload: Predictions from a Model Based on National, Racial, and Ethnic Group Composition in Central Alabama

5. Inheritance of two HFE mutations in African Americans: Cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency

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1. Hereditary Hemochromatosis: Missed Diagnosis or Misdiagnosis?;The American Journal of Medicine;2013-11

2. Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS study initial screening;American Journal of Hematology;2008-02

3. Directions for clinical practice improvement in HFE gene mutation testing;Medical Journal of Australia;2007-09

4. Clinical utility and outcome of HFE-genotyping in the search for hereditary hemochromatosis;Clinica Chimica Acta;2003-05

5. HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFEC282Y homozygosity in central Alabama;BMC Medical Genetics;2002-10-07