These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
338 related articles for article (PubMed ID: 1822787)
21. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype. De Jonghe P; Timmerman V; Nelis E; De Vriendt E; Löfgren A; Ceuterick C; Martin JJ; Van Broeckhoven C Arch Neurol; 1999 Oct; 56(10):1283-8. PubMed ID: 10520946 [TBL] [Abstract][Full Text] [Related]
22. Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplication. Nicholson GA; Kennerson ML; Keats BJ; Mesterovic N; Churcher W; Barker D; Ross DA Am J Med Genet; 1992 Nov; 44(4):455-60. PubMed ID: 1442887 [TBL] [Abstract][Full Text] [Related]
23. The phenotypic manifestations of chromosome 17p11.2 duplication. Thomas PK; Marques W; Davis MB; Sweeney MG; King RH; Bradley JL; Muddle JR; Tyson J; Malcolm S; Harding AE Brain; 1997 Mar; 120 ( Pt 3)():465-78. PubMed ID: 9126058 [TBL] [Abstract][Full Text] [Related]
24. Charcot-Marie-Tooth disease and related inherited neuropathies. Murakami T; Garcia CA; Reiter LT; Lupski JR Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346 [TBL] [Abstract][Full Text] [Related]
26. [The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1]. Bort S; Sevilla T; Vílchez JJ; Prieto F; Palau F Med Clin (Barc); 1995 May; 104(17):648-52. PubMed ID: 7623491 [TBL] [Abstract][Full Text] [Related]
27. [Genotype-phenotype correlation in hereditary motor-sensory neuropathy type IA associated with duplication in chromosome 17p11.2-12]. Ryniewicz B; Jedrzejowska H; Kochański A Neurol Neurochir Pol; 2000; 34(6):1145-53. PubMed ID: 11317491 [TBL] [Abstract][Full Text] [Related]
28. Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2. Holmberg BH; Holmgren G; Nelis E; van Broeckhoven C; Westerberg B J Med Genet; 1994 Jun; 31(6):435-41. PubMed ID: 8071969 [TBL] [Abstract][Full Text] [Related]
29. [Analysis of mutations in the chromosome 17p11.2 region in patients with Charcot-Marie-Tooth type 1 disease and in patients with tomaculous neuropathy]. Zamurović N; Milić V; Dacković J; Zamurović D; Culjković B; Parlović S; Apostolski S; Romac S Srp Arh Celok Lek; 2002; 130(3-4):59-63. PubMed ID: 12154515 [TBL] [Abstract][Full Text] [Related]
30. De novo mutation of Charcot-Marie-Tooth disease type 1A. Tachi N; Kozuka N; Ohya K; Chiba S Pediatr Neurol; 1997 Jul; 17(1):67-9. PubMed ID: 9308980 [TBL] [Abstract][Full Text] [Related]
31. A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients. Silander K; Meretoja P; Nelis E; Timmerman V; Van Broeckhoven C; Aula P; Savontaus ML Hum Mutat; 1996; 8(4):304-10. PubMed ID: 8956034 [TBL] [Abstract][Full Text] [Related]
33. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects]. Hertz MJ; Jensen AD; Brandt CA; Bisgård C Ugeskr Laeger; 1995 Jun; 157(25):3613-8. PubMed ID: 7652980 [TBL] [Abstract][Full Text] [Related]
34. Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus. Chance PF; Matsunami N; Lensch W; Smith B; Bird TD Neurology; 1992 Oct; 42(10):2037-41. PubMed ID: 1407588 [TBL] [Abstract][Full Text] [Related]
35. Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Palau F; Löfgren A; De Jonghe P; Bort S; Nelis E; Sevilla T; Martin JJ; Vilchez J; Prieto F; Van Broeckhoven C Hum Mol Genet; 1993 Dec; 2(12):2031-5. PubMed ID: 8111370 [TBL] [Abstract][Full Text] [Related]
36. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969 [TBL] [Abstract][Full Text] [Related]