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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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I H Scheinberg

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The Journal of Clinical Investigation|November 1, 1989

Hepatocellular copper toxicity and its attenuation by zincM L Schilsky, R R Blank, M J Czaja, et al.

Human Molecular Genetics|August 11, 1999

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformationO I Buiakova, J Xu, S Lutsenko, et al.

Lancet (London, England)|March 13, 1971

Orthotopic liver transplantation for Wilson's diseaseR S DuBois, D O Rodgerson, G Martineau, et al.

American Journal of Human Genetics|November 1, 1988

Eight closely linked loci place the Wilson disease locus within 13q14-q21A M Bowcock, L A Farrer, J M Hebert, et al.

American Journal of Human Genetics|October 1, 1993

Polymorphic microsatellites and Wilson disease (WD)E A Stewart, A White, J Tomfohrde, et al.

The Journal of Clinical Investigation|October 1, 1987

Molecular studies of ceruloplasmin deficiency in Wilson's diseaseM J Czaja, F R Weiner, S J Schwarzenberg, et al.

American Journal of Human Genetics|August 1, 1997

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analysesA B Shah, I Chernov, H T Zhang, et al.

Pageof 8

Search research articles

Showing results (71-80 of 77) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 77 results.

The Journal of Clinical Investigation|November 1, 1989

Hepatocellular copper toxicity and its attenuation by zincM L Schilsky, R R Blank, M J Czaja, et al.

Human Molecular Genetics|August 11, 1999

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformationO I Buiakova, J Xu, S Lutsenko, et al.

Lancet (London, England)|March 13, 1971

Orthotopic liver transplantation for Wilson's diseaseR S DuBois, D O Rodgerson, G Martineau, et al.

American Journal of Human Genetics|November 1, 1988

Eight closely linked loci place the Wilson disease locus within 13q14-q21A M Bowcock, L A Farrer, J M Hebert, et al.

American Journal of Human Genetics|October 1, 1993

Polymorphic microsatellites and Wilson disease (WD)E A Stewart, A White, J Tomfohrde, et al.

The Journal of Clinical Investigation|October 1, 1987

Molecular studies of ceruloplasmin deficiency in Wilson's diseaseM J Czaja, F R Weiner, S J Schwarzenberg, et al.

American Journal of Human Genetics|August 1, 1997

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analysesA B Shah, I Chernov, H T Zhang, et al.

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