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.
116 related articles for article (PubMed ID: 7666403)
21. Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome. Chevillard C; Le Paslier D; Passage E; Ougen P; Billault A; Boyer S; Mazan S; Bachellerie JP; Vignal A; Cohen D Hum Mol Genet; 1993 Aug; 2(8):1235-43. PubMed ID: 8401506 [TBL] [Abstract][Full Text] [Related]
22. Charcot-Marie-Tooth disease type 1A: a family study with microsatellites. Qu Y; Carpenter NJ; Whetsell L; Smith SP; Say B J Okla State Med Assoc; 1996 Nov; 89(11):395-9. PubMed ID: 8972170 [TBL] [Abstract][Full Text] [Related]
23. Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. Matsunami N; Smith B; Ballard L; Lensch MW; Robertson M; Albertsen H; Hanemann CO; Müller HW; Bird TD; White R Nat Genet; 1992 Jun; 1(3):176-9. PubMed ID: 1303231 [TBL] [Abstract][Full Text] [Related]
24. Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group. Brice A; Ravisé N; Stevanin G; Gugenheim M; Bouche P; Penet C; Agid Y J Med Genet; 1992 Nov; 29(11):807-12. PubMed ID: 1453432 [TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A. Kashork CD; Chen KS; Lupski JR; Shaffer LG Ann N Y Acad Sci; 1999 Sep; 883():457-9. PubMed ID: 10586272 [TBL] [Abstract][Full Text] [Related]
26. Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families. MacMillan JC; Upadhyaya M; Harper PS J Med Genet; 1992 Jan; 29(1):12-3. PubMed ID: 1552536 [TBL] [Abstract][Full Text] [Related]
27. Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. Raeymaekers P; Timmerman V; Nelis E; Van Hul W; De Jonghe P; Martin JJ; Van Broeckhoven C J Med Genet; 1992 Jan; 29(1):5-11. PubMed ID: 1552545 [TBL] [Abstract][Full Text] [Related]
28. Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2. Vance JM; Barker D; Yamaoka LH; Stajich JM; Loprest L; Hung WY; Fischbeck K; Roses AD; Pericak-Vance MA Genomics; 1991 Apr; 9(4):623-8. PubMed ID: 1674726 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy. Roa BB; Greenberg F; Gunaratne P; Sauer CM; Lubinsky MS; Kozma C; Meck JM; Magenis RE; Shaffer LG; Lupski JR Hum Genet; 1996 May; 97(5):642-9. PubMed ID: 8655146 [TBL] [Abstract][Full Text] [Related]
31. Charcot-Marie-Tooth disease type 1A duplication by PCR analysis. Tachi N; Kozuka N; Ohya K; Chiba S Pediatr Neurol; 1999 May; 20(5):360-3. PubMed ID: 10371381 [TBL] [Abstract][Full Text] [Related]
33. Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations. Ou Z; Jarmuz M; Sparagana SP; Michaud J; Décarie JC; Yatsenko SA; Nowakowska B; Furman P; Shaw CA; Shaffer LG; Lupski JR; Chinault AC; Cheung SW; Stankiewicz P Hum Genet; 2006 Sep; 120(2):227-37. PubMed ID: 16791615 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies. Stronach EA; Clark C; Bell C; Löfgren A; McKay NG; Timmerman V; Van Broeckhoven C; Haites NE J Peripher Nerv Syst; 1999; 4(2):117-22. PubMed ID: 10442687 [TBL] [Abstract][Full Text] [Related]
36. Facilitated diagnosis of CMT1A duplication in chromosome 17p11.2-12: analysis with a CMT1A-REP repeat probe and photostimulated luminescence imaging. Ikegami T; Ikeda H; Chance PF; Kiyosawa H; Yamamoto M; Sobue G; Ohnishi A; Tachi N; Hayasaka K Hum Mutat; 1997; 9(6):563-6. PubMed ID: 9195231 [TBL] [Abstract][Full Text] [Related]
37. The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A. Valentijn LJ; Bolhuis PA; Zorn I; Hoogendijk JE; van den Bosch N; Hensels GW; Stanton VP; Housman DE; Fischbeck KH; Ross DA Nat Genet; 1992 Jun; 1(3):166-70. PubMed ID: 1303229 [TBL] [Abstract][Full Text] [Related]
38. The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Timmerman V; Nelis E; Van Hul W; Nieuwenhuijsen BW; Chen KL; Wang S; Ben Othman K; Cullen B; Leach RJ; Hanemann CO Nat Genet; 1992 Jun; 1(3):171-5. PubMed ID: 1303230 [TBL] [Abstract][Full Text] [Related]
39. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Patel PI; Roa BB; Welcher AA; Schoener-Scott R; Trask BJ; Pentao L; Snipes GJ; Garcia CA; Francke U; Shooter EM; Lupski JR; Suter U Nat Genet; 1992 Jun; 1(3):159-65. PubMed ID: 1303228 [TBL] [Abstract][Full Text] [Related]
40. Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17. Kaku DA; Parry GJ; Malamut R; Lupski JR; Garcia CA Neurology; 1993 Sep; 43(9):1806-8. PubMed ID: 8414036 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]