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.
8. De novo partial duplication of 17p associated with Charcot-Marie-Tooth disease type 1A. Fernández-Torre JL; Otero B; Alvarez V; Hernando I; Fernández-Toral J J Neurol Neurosurg Psychiatry; 2001 May; 70(5):703-4. PubMed ID: 11336036 [No Abstract] [Full Text] [Related]
9. 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]
10. Charcot-Marie-Tooth disease type 1. Malcolm S J Med Genet; 1992 Jan; 29(1):3-4. PubMed ID: 1552540 [No Abstract] [Full Text] [Related]
11. New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplication. Bost M; Bonnebouche C; Gonnaud PM; Cochat P; Gilbert B; Dupont C; Chazot G; Vandenberghe A Clin Genet; 1994 Nov; 46(5):380-1. PubMed ID: 7889651 [No Abstract] [Full Text] [Related]
12. Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication. Dupré N; Bouchard JP; Cossette L; Brunet D; Vanasse M; Lemieux B; Mathon G; Puymirat J Ann N Y Acad Sci; 1999 Sep; 883():497-9. PubMed ID: 10586283 [No Abstract] [Full Text] [Related]
13. Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a). Hoogendijk JE; Janssen EA; Gabreëls-Festen AA; Hensels GW; Joosten EM; Gabreëls FJ; Zorn I; Valentijn LJ; Baas F; Ongerboer de Visser BW Neurology; 1993 May; 43(5):1010-5. PubMed ID: 8492918 [TBL] [Abstract][Full Text] [Related]
14. Severe Guillain-Barré syndrome associated with chromosome 17p11.2-12 duplication. Münch C; Epplen JT; Meins M; Meyer R; Weber JR; Meyer T Muscle Nerve; 2008 Feb; 37(2):256-8. PubMed ID: 17763453 [TBL] [Abstract][Full Text] [Related]
15. The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2. Hoogendijk JE; Hensels GW; Zorn I; Valentijn L; Janssen EA; de Visser M; Barker DF; Ongerboer de Visser BW; Baas F; Bolhuis PA Hum Genet; 1991 Dec; 88(2):215-8. PubMed ID: 1721895 [TBL] [Abstract][Full Text] [Related]
17. Roussy-Lévy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome IA associated with a duplication on chromosome 17p11.2. Auer-Grumbach M; Strasser-Fuchs S; Wagner K; Körner E; Fazekas F J Neurol Sci; 1998 Jan; 154(1):72-5. PubMed ID: 9543325 [TBL] [Abstract][Full Text] [Related]
18. Proximal Charcot-Marie-Tooth syndrome with duplication on chromosome 17p11.2. Auer-Grumbach M; Wagner K; Payer F; Hartung HP Ann N Y Acad Sci; 1999 Sep; 883():469-71. PubMed ID: 10586276 [No Abstract] [Full Text] [Related]