Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
Richard, Gabriele, Bale, Sherri J, Smith, Lisa E, Bailey, Regina A, Itin, Peter, Hohl, Daniel, Epstein, Ervin H, DiGiovanna, John J, Compton, John G
Published in Nature genetics (01.12.1998)
Published in Nature genetics (01.12.1998)
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Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma
RICHARD, G, WHITE, T. W, SMITH, L. E, BAILEY, R. A, COMPTON, J. G, PAUL, D. L, BALE, S. J
Published in Human genetics (01.10.1998)
Published in Human genetics (01.10.1998)
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The spectrum of mutations in erythrokeratodermias - novel and de novo mutations in GJB3
Richard, G., Brown, N., Smith, L.E., Terrinoni, A., Melino, G., MacKie, R.M., Bale, S.J., Uitto, J.
Published in Human genetics (30.03.2000)
Published in Human genetics (30.03.2000)
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Commodity supply and use balances and food availability
El Obeid, Amani E.; Johnson, Stanley R.; Smith, Lisa C.; Jensen, Helen H
Year of Publication 23.03.2012
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Year of Publication 23.03.2012
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