Shanxiang Zhang, Ph.D.
Affiliations: | 2001 | Ohio State University, Columbus, Columbus, OH |
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GeneticsGoogle:
"Shanxiang Zhang"Mean distance: 53433
Parents
Sign in to add mentor| Ralf Krahe | grad student | 2001 | Ohio State | |
| (Positional cloning of a novel heritable, rare, folate -sensitive fragile site (FRAXG) in Xp22.1 associated with short stature in a Finnish kindred and cloning of an associated candidate gene (FXGAG).) | ||||
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Publications
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| Grewal RP, Zhang S, Ma W, et al. (2004) Clinical and genetic analysis of a family with PROMM. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 11: 603-5 |
| Sallinen R, Vihola A, Bachinski LL, et al. (2004) New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscular Disorders : Nmd. 14: 274-83 |
| Meola G, Sansone V, Perani D, et al. (2003) Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2). Neuromuscular Disorders : Nmd. 13: 813-21 |
| Bachinski LL, Udd B, Meola G, et al. (2003) Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect. American Journal of Human Genetics. 73: 835-48 |
| Vihola A, Bassez G, Meola G, et al. (2003) Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology. 60: 1854-7 |
| Zhang S, Krahe R. (2002) Physical and transcript map of a 2-Mb region in Xp22.1 containing candidate genes for X-linked mental retardation and short stature. Genomics. 79: 274-7 |