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American Journal of Medical Genetics|November 15, 1993
Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndromeK A Ellison, E J Roth, E R McCabe, et al.
Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Spinocerebellar ataxia type 1H Y Zoghbi
Bailliere'S Clinical Neurology|August 1, 1994
Molecular genetics of hereditary ataxiasS Banfi, H Y Zoghbi
Annual Review of Physiology|June 9, 2000
Insights from mouse models into the molecular basis of neurodegenerationN Heintz, H Y Zoghbi
American Journal of Human Genetics|February 1, 1992
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisK A Ellison, C P Fill, J Terwilliger, et al.
Seminars in Cell Biology|February 1, 1995
Spinocerebellar ataxia type 1H Y Zoghbi, H T Orr
Annual Review of Neuroscience|June 9, 2000
Glutamine repeats and neurodegenerationH Y Zoghbi, H T Orr
Current Opinion in Pediatrics|December 1, 1995
Trinucleotide repeat disorders in pediatricsD M O'Donnell, H Y Zoghbi
Current Opinion in Neurobiology|October 6, 1999
Polyglutamine diseases: protein cleavage and aggregationH Y Zoghbi, H T Orr
Human Molecular Genetics|April 18, 2000
Fourteen and counting: unraveling trinucleotide repeat diseasesC J Cummings, H Y Zoghbi
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