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Publications by Alain Meyrier

Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44

American Journal of Human Genetics
Genetics
1999English

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Muckle–Wells Syndrome in a Child With Recurrent Urticaria

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Genetic Linkage of Meleda Disease to Chromosome 8qter

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IL-1 Inhibition in Muckle-Wells-Syndrome: Withdrawal Resulting in Rapid Deterioration of Hearing Loss

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Mutation of a New Gene Encoding a Putative Pyrin-Like Protein Causes Familial Cold Autoinflammatory Syndrome and Muckle–Wells Syndrome

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Linkage of Essential Hypertension to Chromosome 18q

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Integrating Genetic Linkage Maps With Pachytene Chromosome Structure in Maize

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Genetic Linkage of Autosomal Dominant Primary Open Angle Glaucoma to Chromosome 3q in a Greek Pedigree

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Linkage Mapping of Ovine Microphthalmia to Chromosome 23, the Sheep Orthologue of Human Chromosome 18

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Linkage of the Wiskott-Aldrich Syndrome With Polymorphic DNA Sequences From the Human X Chromosome.

Proceedings of the National Academy of Sciences of the United States of America
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