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Human Molecular Genetics|December 1, 1992
The genomic organization of a novel regulatory myosin light chain gene (MYL5) that maps to chromosome 4p16.3 and shows different patterns of expression between primatesC Collins, K Schappert, M R HaydenBrain Pathology (Zurich, Switzerland)|October 1, 1992
New insights into the clinical features, pathogenesis and molecular genetics of Huntington diseaseB Kremer, B Weber, M R HaydenClinical Genetics|January 6, 2011
Adoption and the communication of genetic risk: experiences in Huntington diseaseY Bombard, A Semaka, M R HaydenCurrent Opinion in Neurology|August 1, 1994
The molecular genetics of Huntington's diseaseY P Goldberg, H Telenius, M R HaydenAmerican Journal of Human Genetics|July 1, 1988
Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH)S Langlois, J J Kastelein, M R HaydenHuman Molecular Genetics|January 1, 1996
Huntington disease: new insights into the relationship between CAG expansion and diseaseJ Nasir, Y P Goldberg, M R HaydenJournal of Genetic Counseling|August 21, 2012
"Grasping the grey": patient understanding and interpretation of an intermediate allele predictive test result for Huntington diseaseA Semaka, L G Balneaves, M R HaydenAmerican Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles)A Semaka, J A Collins, M R HaydenClinical Genetics|August 1, 1985
Age of onset in siblings of persons with juvenile Huntington diseaseM R Hayden, J A Soles, R H WardSouth African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 2, 1980
The prevalence of Huntington's chorea in South AfricaM R Hayden, J M MacGregor, P H BeightonPageof 34