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Genetic Testing|April 1, 2008
New mutations in the Wilson disease gene, ATP7B: implications for molecular testingLisa Prat Davies, Georgina Macintyre, Diane W CoxAmerican Journal of Medical Genetics. Part A|December 13, 2007
A child with deletion (14)(q24.3q32.13) and auditory neuropathyKamilla Schlade-Bartusiak, Georgina Macintyre, Janice Zunich, et al.Human Mutation|March 25, 2010
Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7BLeiah M Luoma, Taha M M Deeb, Georgina Macintyre, et al.The Journal of Laboratory and Clinical Medicine|December 23, 2004
Value of an enzymatic assay for the determination of serum ceruloplasminGeorgina Macintyre, Klaus S Gutfreund, W R Wayne Martin, et al.Schizophrenia Research|May 15, 2010
Association of NPAS3 exonic variation with schizophreniaGeorgina Macintyre, Tyler Alford, Lan Xiong, et al.Biochimie|June 23, 2009
A minigene approach for analysis of ATP7B splice variants in patients with Wilson diseaseAnna M E Wilson, Kamilla Schlade-Bartusiak, Jean-Luc Tison, et al.Human Mutation|January 19, 2008
Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model systemGloria Hsi, Lara M Cullen, Georgina Macintyre, et al.BMC Medical Genetics|March 29, 2014
NPAS3 variants in schizophrenia: a neuroimaging studyDenise Bernier, Georgina Macintyre, Robert Bartha, et al.Viruses|May 28, 2022
Isolation of a Human Betaretrovirus from Patients with Primary Biliary CholangitisMariam Goubran, Weiwei Wang, Stanislav Indik, et al.Psychiatry Research|August 25, 2019
Trend level gene-gender interaction effect for the BDNF rs6265 variant on age of onset of psychosisRohit J Lodhi, Yabing Wang, Georgina Macintyre, et al.Pageof 2