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.
44. Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B). Gambardella A; Bolino A; Muglia M; Valentino P; Bono F; Oliveri RL; Sabatelli M; Brancolini V; Van Broeckhoven C; Romeo G; Devoto M; Quattrone A Neurology; 1998 Mar; 50(3):799-801. PubMed ID: 9521281 [TBL] [Abstract][Full Text] [Related]
45. 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]
46. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. Bird TD; Ott J; Giblett ER Am J Hum Genet; 1982 May; 34(3):388-94. PubMed ID: 6952764 [TBL] [Abstract][Full Text] [Related]
47. Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth. Sevilla T; Martínez-Rubio D; Márquez C; Paradas C; Colomer J; Jaijo T; Millán JM; Palau F; Espinós C Clin Genet; 2013 Jun; 83(6):565-70. PubMed ID: 22978647 [TBL] [Abstract][Full Text] [Related]
48. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Evgrafov OV; Mersiyanova I; Irobi J; Van Den Bosch L; Dierick I; Leung CL; Schagina O; Verpoorten N; Van Impe K; Fedotov V; Dadali E; Auer-Grumbach M; Windpassinger C; Wagner K; Mitrovic Z; Hilton-Jones D; Talbot K; Martin JJ; Vasserman N; Tverskaya S; Polyakov A; Liem RK; Gettemans J; Robberecht W; De Jonghe P; Timmerman V Nat Genet; 2004 Jun; 36(6):602-6. PubMed ID: 15122254 [TBL] [Abstract][Full Text] [Related]
49. 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]
50. Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene. Delague V; Bareil C; Tuffery S; Bouvagnet P; Chouery E; Koussa S; Maisonobe T; Loiselet J; Mégarbané A; Claustres M Am J Hum Genet; 2000 Jul; 67(1):236-43. PubMed ID: 10848494 [TBL] [Abstract][Full Text] [Related]
52. [Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Liu XX; Duan XH; Zhang S; Sun AP; Zhang YS; Fan DS Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Oct; 54(5):874-883. PubMed ID: 36241230 [TBL] [Abstract][Full Text] [Related]
53. Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1. Verhoeven K; Villanova M; Rossi A; Malandrini A; De Jonghe P; Timmerman V Am J Hum Genet; 2001 Oct; 69(4):889-94. PubMed ID: 11533914 [TBL] [Abstract][Full Text] [Related]
54. 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]
55. 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]
56. Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1. Guiloff RJ; Thomas PK; Contreras M; Armitage S; Schwarz G; Sedgwick EM J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):669-74. PubMed ID: 7130990 [TBL] [Abstract][Full Text] [Related]
58. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies. Verhalle D; Löfgren A; Nelis E; Dehaene I; Theys P; Lammens M; Dom R; Van Broeckhoven C; Robberecht W Ann Neurol; 1994 Jun; 35(6):704-8. PubMed ID: 8210227 [TBL] [Abstract][Full Text] [Related]
59. 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]
60. 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] [Previous] [Next] [New Search]