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3. A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2. Lo Nigro C, Cusano R, Scaranari M, Cinti R, Forabosco P, Morra VB, De Michele G, Santoro L, Davies S, Hurst J, Devoto M, Ravazzolo R, Seri M. Eur J Hum Genet; 2000 Oct; 8(10):777-82. PubMed ID: 11039578 [Abstract] [Full Text] [Related]
5. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3. De Michele G, De Fusco M, Cavalcanti F, Filla A, Marconi R, Volpe G, Monticelli A, Ballabio A, Casari G, Cocozza S. Am J Hum Genet; 1998 Jul; 63(1):135-9. PubMed ID: 9634528 [Abstract] [Full Text] [Related]
6. A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13. Reid E, Dearlove AM, Osborn O, Rogers MT, Rubinsztein DC. Am J Hum Genet; 2000 Feb; 66(2):728-32. PubMed ID: 10677333 [Abstract] [Full Text] [Related]
7. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity. Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC. Neurology; 1999 Nov 10; 53(8):1844-9. PubMed ID: 10563637 [Abstract] [Full Text] [Related]
8. Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia. Speer MC, Kingston HM, Boustany RM, Gaskell PC, Robinson LC, Lennon F, Wolpert CM, Yamaoka LH, Kahler SG, Hogan EL. Am J Med Genet; 1995 Aug 14; 60(4):307-11. PubMed ID: 7485266 [Abstract] [Full Text] [Related]
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19. Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom families. Reid E, Grayson C, Rogers MT, Rubinsztein DC. Brain; 1999 Sep 14; 122 ( Pt 9)():1741-55. PubMed ID: 10468513 [Abstract] [Full Text] [Related]
20. Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1. Zortea M, Vettori A, Trevisan CP, Bellini S, Vazza G, Armani M, Simonati A, Mostacciuolo ML. J Med Genet; 2002 Jun 14; 39(6):387-90. PubMed ID: 12070243 [Abstract] [Full Text] [Related] Page: [Next] [New Search]