J. L. Gall

发表

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

J. J. Pointon, J. Crowe, P. Gasparini, 1999, Nature Genetics.

Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis

P. Pontarotti, A. Kahloun, J. Yaouanq, 1992, Human Genetics.

HLA class I gene polymorphism in genetic hemochromatosis

R. Fauchet, J. Yaouanq, M. Blayau, 1990, Human Genetics.

Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)

B. Chauvel, J. Yaouanq, J. Feingold, 2004, Human Genetics.

Haemochromatosis and HLA–H

P. Fergelot, J. Mosser, I. Gicquel, 1996, Nature Genetics.

Bf Polymorphism Studied by Isoelectrofocusing

R. Fauchet, V. David, M. Guéguen, 1984 .

Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20

S. Odent, H. Journel, M. Blayau, 1993, Human Genetics.

Cloning of a human homologue of the mouseTctex-5 gene within theMHC class I region

P. Pontarotti, P. Jézéquel, M. Lepourcelet, 2007, Immunogenetics.

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations

P. Fergelot, J. Yaouanq, V. David, 1997, Human Genetics.

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

I. Gicquel, R. Fauchet, M. Simon, 1986, Human Genetics.

Ferritin H gene polymorphism in idiopathic hemochromatosis

M. Simon, L. Abel, J. Yaouanq, 2004, Human Genetics.

A human homologue to the yeast omnipotent suppressor 45 maps 100 kb centromeric to HLA-A

P. Fergelot, I. Gicquel, B. Chauvel, 1995, Immunogenetics.