Showing results (31-40 of 63) with videos related to
Sort By:
Pageof 7
Neurology|May 10, 2000
The DYT1 phenotype and guidelines for diagnostic testingS B Bressman, C Sabatti, D Raymond, et al.Nature|March 17, 1988
Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinomaB R Seizinger, G A Rouleau, L J Ozelius, et al.JIMD Reports|May 23, 2014
Cognitive and Antipsychotic Medication Use in Monoallelic GBA-Related Parkinson DiseaseM J Barrett, V L Shanker, W L Severt, et al.Neurology|December 1, 1993
Rapid-onset dystonia-parkinsonismW B Dobyns, L J Ozelius, P L Kramer, et al.American Journal of Human Genetics|March 1, 1992
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi JewsL J Ozelius, P L Kramer, D de Leon, et al.Neurology|February 14, 2007
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriersC W Hess, D Raymond, P de Carvalho Aguiar, et al.Annals of Neurology|August 12, 1999
Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13P L Kramer, M Mineta, C Klein, et al.American Journal of Human Genetics|January 1, 1989
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1)B R Seizinger, G E Farmer, J L Haines, et al.Genomics|December 1, 1987
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17B R Seizinger, G A Rouleau, A H Lane, et al.Neurology|February 1, 1994
A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneityS B Bressman, G A Heiman, T G Nygaard, et al.Pageof 7