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Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Population based study of late onset cerebellar ataxia in south east WalesM B Muzaimi, J Thomas, S Palmer-Smith, et al.AJR. American Journal of Roentgenology|December 1, 1987
Hemorrhagic neoplasms: MR mimics of occult vascular malformationsG Sze, G Krol, W L Olsen, et al.Clinical Oncology (Royal College of Radiologists (Great Britain))|December 14, 2020
Identifying Risk Factors for Anthracycline Chemotherapy-induced Phlebitis in Women with Breast Cancer: An Observational StudyR Roberts, A Borley, L Hanna, et al.Human Genetics|January 1, 1983
Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophyM Sarfarazi, P S Harper, H M Kingston, et al.American Journal of Human Genetics|September 28, 2000
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helixA J Richards, D M Baguley, J R Yates, et al.Genomics|November 1, 1992
Genetic heterogeneity in X-linked amelogenesis imperfectaM J Aldred, P J Crawford, E Roberts, et al.Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.Neuromuscular Disorders : NMD|November 26, 1998
PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafnessM F Phillips, M T Rogers, R Barnetson, et al.Pageof 30