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M R Hayden

Showing results (101-110 of 342) with videos related to

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American Journal of Medical Genetics|July 1, 1989
Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosaR B Lowry, B J Wood, T A Cox, et al.
Clinical Genetics|October 9, 2012
Providing predictive testing for Huntington disease via telehealth: results of a pilot study in British Columbia, CanadaA K Hawkins, S Creighton, A Ho, et al.
Clinical Biochemistry|April 1, 1985
Urinary proteins in a patient with Tangier diseaseP H Pritchard, M Bergseth, R McLeod, et al.
Brain Research|March 20, 1999
Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease geneJ R O'Kusky, J Nasir, F Cicchetti, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|December 1, 1986
Regression model for predicting dissociations of regional cerebral glucose metabolism in individuals at risk for Huntington's diseaseC M Clark, M R Hayden, A J Stoessl, et al.
Human Molecular Genetics|June 1, 1993
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington diseaseY P Goldberg, S E Andrew, L A Clarke, et al.
Journal of Medical Genetics|April 1, 1982
The high frequency of juvenile Huntington's chorea in South AfricaM R Hayden, J M MacGregor, D S Saffer, et al.
Journal of Medical Genetics|June 1, 1989
Different options for prenatal testing for Huntington's disease using DNA probesM Fahy, C Robbins, M Bloch, et al.
Southern Medical Journal|September 1, 1990
Corticosteroid treatment of hemolytic anemia associated with Mycoplasma pneumoniae pneumoniaC S Chu, S R Braun, J W Yarbro, et al.
Molecular Biology & Medicine|December 1, 1990
Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiencyH E Henderson, R Devlin, J Peterson, et al.
Pageof 35

Showing results (101-110 of 342) with videos related to

Sort By:
Pageof 35
American Journal of Medical Genetics|July 1, 1989
Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosaR B Lowry, B J Wood, T A Cox, et al.
Clinical Genetics|October 9, 2012
Providing predictive testing for Huntington disease via telehealth: results of a pilot study in British Columbia, CanadaA K Hawkins, S Creighton, A Ho, et al.
Clinical Biochemistry|April 1, 1985
Urinary proteins in a patient with Tangier diseaseP H Pritchard, M Bergseth, R McLeod, et al.
Brain Research|March 20, 1999
Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease geneJ R O'Kusky, J Nasir, F Cicchetti, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|December 1, 1986
Regression model for predicting dissociations of regional cerebral glucose metabolism in individuals at risk for Huntington's diseaseC M Clark, M R Hayden, A J Stoessl, et al.
Human Molecular Genetics|June 1, 1993
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington diseaseY P Goldberg, S E Andrew, L A Clarke, et al.
Journal of Medical Genetics|April 1, 1982
The high frequency of juvenile Huntington's chorea in South AfricaM R Hayden, J M MacGregor, D S Saffer, et al.
Journal of Medical Genetics|June 1, 1989
Different options for prenatal testing for Huntington's disease using DNA probesM Fahy, C Robbins, M Bloch, et al.
Southern Medical Journal|September 1, 1990
Corticosteroid treatment of hemolytic anemia associated with Mycoplasma pneumoniae pneumoniaC S Chu, S R Braun, J W Yarbro, et al.
Molecular Biology & Medicine|December 1, 1990
Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiencyH E Henderson, R Devlin, J Peterson, et al.
Pageof 35