Concepedia

Mutation in the Gene for Connexin 30.3 in a Family with Erythrokeratodermia Variabilis

Françoise Macari, Marina Landau, Pascal Cousin, B. Mevorah, Sarah Brenner, Renato G. Panizzon, Daniel F. Schorderet, Daniel Hohl, Marcel Huber

The American Journal of Human Genetics · 2000 · 159 citations · 19 references

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References

19

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Colette Dib, Sabine Fauré, Cécile Fizames et al. · Nature · 1996 · 3K citations

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Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

, , +16

Online Mendelian Inheritance in Man 'OMIM'.

Sangeeta Amladi · PubMed · 2007 · 870 citations · Full text

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Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

Gabriele Richard, Lisa E. Smith, Regina A. Bailey et al. · Nature Genetics · 1998 · 345 citations

, , +3

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

X.Z. Liu · Human Molecular Genetics · 2000 · 185 citations

, , +15