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P J Lockhart

Showing results (31-40 of 39) with videos related to

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Journal of Medical Genetics|February 27, 2004
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein functionP J Lockhart, S Lincoln, M Hulihan, et al.
Immunology and Cell Biology|October 1, 1996
Cloning of novel kinectin splice variants with alternative C-termini: structure, distribution and evolution of mouse kinectinE Leung, C G Print, D A Parry, et al.
Molecular Biology and Evolution|April 26, 2000
How molecules evolve in eubacteriaP J Lockhart, D Huson, U Maier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
JIMD Reports|April 15, 2018
Severe Leukoencephalopathy with Clinical Recovery Caused by Recessive BOLA3 MutationsC A Stutterd, N J Lake, H Peters, et al.
Clinical Genetics|November 26, 2009
Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schoolsM B Delatycki, M Wolthuizen, V Collins, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genesA B West, A Zimprich, P J Lockhart, et al.
The Journal of Biological Chemistry|November 13, 1998
Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPasesS L La Fontaine, S D Firth, J Camakaris, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Journal of Medical Genetics|February 27, 2004
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein functionP J Lockhart, S Lincoln, M Hulihan, et al.
Immunology and Cell Biology|October 1, 1996
Cloning of novel kinectin splice variants with alternative C-termini: structure, distribution and evolution of mouse kinectinE Leung, C G Print, D A Parry, et al.
Molecular Biology and Evolution|April 26, 2000
How molecules evolve in eubacteriaP J Lockhart, D Huson, U Maier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2005
Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG geneM C Fahey, M A Knight, J H Shaw, et al.
JIMD Reports|April 15, 2018
Severe Leukoencephalopathy with Clinical Recovery Caused by Recessive BOLA3 MutationsC A Stutterd, N J Lake, H Peters, et al.
Clinical Genetics|November 26, 2009
Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schoolsM B Delatycki, M Wolthuizen, V Collins, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genesA B West, A Zimprich, P J Lockhart, et al.
The Journal of Biological Chemistry|November 13, 1998
Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPasesS L La Fontaine, S D Firth, J Camakaris, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
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