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M L Franz

Showing results (11-20 of 21) with videos related to

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Journal of Medical Genetics|February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expressionR L Margolis, O C Stine, C M Ward, et al.
Annals of Neurology|January 5, 2002
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansionR L Margolis, E O'Hearn, A Rosenblatt, et al.
Annals of Neurology|September 18, 2001
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansionR L Margolis, E O'Hearn, A Rosenblatt, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
JAMA|June 2, 1989
Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's diseaseJ Brandt, K A Quaid, S E Folstein, et al.
Science (New York, N.Y.)|August 23, 1985
Huntington's disease: two families with differing clinical features show linkage to the G8 probeS E Folstein, J A Phillips, D A Meyers, et al.
Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expressionR L Margolis, O C Stine, C M Ward, et al.
Annals of Neurology|January 5, 2002
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansionR L Margolis, E O'Hearn, A Rosenblatt, et al.
Annals of Neurology|September 18, 2001
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansionR L Margolis, E O'Hearn, A Rosenblatt, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
JAMA|June 2, 1989
Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's diseaseJ Brandt, K A Quaid, S E Folstein, et al.
Science (New York, N.Y.)|August 23, 1985
Huntington's disease: two families with differing clinical features show linkage to the G8 probeS E Folstein, J A Phillips, D A Meyers, et al.
Neuron|November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissuesS H Li, G Schilling, W S Young, et al.
American Journal of Medical Genetics|July 13, 2001
Familial influence on age of onset among siblings with Huntington diseaseA Rosenblatt, R R Brinkman, K Y Liang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 1, 1997
Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigreesM W Becher, D C Rubinsztein, J Leggo, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
Pageof 3