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Journal of Medical Genetics|December 1, 1993
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary choreaJ C MacMillan, P J Morrison, N C Nevin, et al.The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.The British Journal of Ophthalmology|May 1, 1985
A genetic linkage study of a kindred with X-linked retinitis pigmentosaS S Bhattacharya, J F Clayton, P S Harper, et al.Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.Journal of Medical Genetics|February 1, 1991
Identification of new DNA markers close to the myotonic dystrophy locusJ D Brook, H G Harley, K V Walsh, et al.Human Genetics|May 1, 1993
Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12M Upadhyaya, S H Roberts, J Farnham, et al.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.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.Pageof 23