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.
164 related articles for article (PubMed ID: 2895983)
41. Linkage between the loci for autosomal dominant Charcot-Marie-Tooth neuropathy type 1 and human glucocerebrosidase. Ionasescu V; Burns T; Ionasescu R; Searby C; Ginns E Cytogenet Cell Genet; 1988; 47(3):173-4. PubMed ID: 3163969 [No Abstract] [Full Text] [Related]
42. X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq. Gal A; Mücke J; Theile H; Wieacker PF; Ropers HH; Wienker TF Hum Genet; 1985; 70(1):38-42. PubMed ID: 2987105 [TBL] [Abstract][Full Text] [Related]
43. X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region. Mostacciuolo ML; Müller E; Fardin P; Micaglio GF; Bardoni B; Guioli S; Camerino G; Danieli GA Hum Genet; 1991 May; 87(1):23-7. PubMed ID: 1674715 [TBL] [Abstract][Full Text] [Related]
45. Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12. Timmerman V; Raeymaekers P; De Jonghe P; De Winter G; Swerts L; Jacobs K; Gheuens J; Martin JJ; Vandenberghe A; Van Broeckhoven C Am J Hum Genet; 1990 Oct; 47(4):680-5. PubMed ID: 2220808 [TBL] [Abstract][Full Text] [Related]
46. Charcot-Marie-Tooth disease: molecular characterization of patients from central and southern Italy. Guzzetta V; Santoro L; Gasparo-Rippa P; Ragno M; Vita G; Caruso G; Andria G Clin Genet; 1995 Jan; 47(1):27-32. PubMed ID: 7774040 [TBL] [Abstract][Full Text] [Related]
47. 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]
48. Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13. Timmerman V; De Jonghe P; Spoelders P; Simokovic S; Löfgren A; Nelis E; Vance J; Martin JJ; Van Broeckhoven C Neurology; 1996 May; 46(5):1311-8. PubMed ID: 8628473 [TBL] [Abstract][Full Text] [Related]
49. Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15. Sambuughin N; Sivakumar K; Selenge B; Lee HS; Friedlich D; Baasanjav D; Dalakas MC; Goldfarb LG J Neurol Sci; 1998 Nov; 161(1):23-8. PubMed ID: 9879677 [TBL] [Abstract][Full Text] [Related]
50. Charcot-Marie-Tooth neuropathy related to chromosome 1. Ionasescu VV; Trofatter J; Haines JL; Ionasescu R; Searby C Am J Med Genet; 1992 Mar; 42(5):728-32. PubMed ID: 1632448 [TBL] [Abstract][Full Text] [Related]
51. Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy. Ionasescu VV; Trofatter J; Haines JL; Ionasescu R; Searby C Neurology; 1992 Apr; 42(4):903-8. PubMed ID: 1565250 [TBL] [Abstract][Full Text] [Related]
52. Heterogeneity of hereditary motor and sensory neuropathy type I (HMSN I): electroneurographical findings, visual evoked potentials and blood group markers in a family with Charcot-Marie-Tooth disease (CMT). Leblhuber F; Reisecker F; Mayr WR; Deisenhammer E Acta Neurol Scand; 1986 Aug; 74(2):145-9. PubMed ID: 3022527 [TBL] [Abstract][Full Text] [Related]
53. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Chance PF; Fischbeck KH Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745 [TBL] [Abstract][Full Text] [Related]
55. Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1). Hallam PJ; Harding AE; Berciano J; Barker DF; Malcolm S Ann Neurol; 1992 May; 31(5):570-2. PubMed ID: 1596093 [TBL] [Abstract][Full Text] [Related]
56. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Kwon JM; Elliott JL; Yee WC; Ivanovich J; Scavarda NJ; Moolsintong PJ; Goodfellow PJ Am J Hum Genet; 1995 Oct; 57(4):853-8. PubMed ID: 7573046 [TBL] [Abstract][Full Text] [Related]
57. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I). Bird TD; Ott J; Giblett ER; Chance PF; Sumi SM; Kraft GH Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251 [TBL] [Abstract][Full Text] [Related]
58. Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35. Jordanova A; Thomas FP; Guergueltcheva V; Tournev I; Gondim FA; Ishpekova B; De Vriendt E; Jacobs A; Litvinenko I; Ivanova N; Buzhov B; De Jonghe P; Kremensky I; Timmerman V Am J Hum Genet; 2003 Dec; 73(6):1423-30. PubMed ID: 14606043 [TBL] [Abstract][Full Text] [Related]
59. Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A. Saito M; Hayashi Y; Suzuki T; Tanaka H; Hozumi I; Tsuji S Neurology; 1997 Dec; 49(6):1630-5. PubMed ID: 9409358 [TBL] [Abstract][Full Text] [Related]