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Human Genetics
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October 28, 2003
A comparison of the mutation spectra of Menkes disease and Wilson disease
Gloria Hsi, Diane W Cox
Human Mutation
|
August 8, 2007
Sequence variation database for the Wilson disease copper transporter, ATP7B
Susan M Kenney, Diane W Cox
Journal of Bioenergetics and Biomembranes
|
January 24, 2003
Copper transporting P-type ATPases and human disease
Diane W Cox, Steven D P Moore
Nephron
|
October 10, 2002
Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b
Steven D P Moore, Diane W Cox
American Journal of Medical Genetics. Part A
|
April 15, 2009
A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlations
Kamilla Schlade-Bartusiak, Holly Ardinger, Diane W Cox
Genetic Testing
|
April 1, 2008
New mutations in the Wilson disease gene, ATP7B: implications for molecular testing
Lisa Prat Davies, Georgina Macintyre, Diane W Cox
Journal of Hepatology
|
July 17, 2007
Three atypical cases of Wilson disease: assessment of the Leipzig scoring system in making a diagnosis
Andy Xuan, Ian Bookman, Diane W Cox, et al.
Veterinary Journal (London, England : 1997)
|
June 19, 2007
Polymorphisms in canine ATP7B: candidate modifier of copper toxicosis in the Bedlington terrier
Veronica A Coronado, Brian O'Neill, Manoj Nanji, et al.
American Journal of Medical Genetics. Part A
|
December 13, 2007
A child with deletion (14)(q24.3q32.13) and auditory neuropathy
Kamilla Schlade-Bartusiak, Georgina Macintyre, Janice Zunich, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 20, 2003
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis
Veronica A Coronado, Deepti Damaraju, Ritva Kohijoki, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Human Genetics
|
October 28, 2003
A comparison of the mutation spectra of Menkes disease and Wilson disease
Gloria Hsi, Diane W Cox
Human Mutation
|
August 8, 2007
Sequence variation database for the Wilson disease copper transporter, ATP7B
Susan M Kenney, Diane W Cox
Journal of Bioenergetics and Biomembranes
|
January 24, 2003
Copper transporting P-type ATPases and human disease
Diane W Cox, Steven D P Moore
Nephron
|
October 10, 2002
Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b
Steven D P Moore, Diane W Cox
American Journal of Medical Genetics. Part A
|
April 15, 2009
A child with terminal 14q deletion syndrome: consideration of genotype-phenotype correlations
Kamilla Schlade-Bartusiak, Holly Ardinger, Diane W Cox
Genetic Testing
|
April 1, 2008
New mutations in the Wilson disease gene, ATP7B: implications for molecular testing
Lisa Prat Davies, Georgina Macintyre, Diane W Cox
Journal of Hepatology
|
July 17, 2007
Three atypical cases of Wilson disease: assessment of the Leipzig scoring system in making a diagnosis
Andy Xuan, Ian Bookman, Diane W Cox, et al.
Veterinary Journal (London, England : 1997)
|
June 19, 2007
Polymorphisms in canine ATP7B: candidate modifier of copper toxicosis in the Bedlington terrier
Veronica A Coronado, Brian O'Neill, Manoj Nanji, et al.
American Journal of Medical Genetics. Part A
|
December 13, 2007
A child with deletion (14)(q24.3q32.13) and auditory neuropathy
Kamilla Schlade-Bartusiak, Georgina Macintyre, Janice Zunich, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 20, 2003
New haplotypes in the Bedlington terrier indicate complexity in copper toxicosis
Veronica A Coronado, Deepti Damaraju, Ritva Kohijoki, et al.
Page
of 3