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3. Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease. LeGuern E; Gouider R; Mabin D; Tardieu S; Birouk N; Parent P; Bouche P; Brice A Ann Neurol; 1997 Jan; 41(1):104-8. PubMed ID: 9005872 [TBL] [Abstract][Full Text] [Related]
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10. Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1. Numakura C; Lin C; Oka N; Akiguchi I; Hayasaka K Ann Neurol; 2000 Jan; 47(1):101-3. PubMed ID: 10632107 [TBL] [Abstract][Full Text] [Related]
11. [Development of molecular genetics and Charcot-Marie-Tooth disease. Important changes in clinical diagnostics]. Ericson U; Borg K; Anvret M Lakartidningen; 1997 Feb; 94(6):428-30. PubMed ID: 9053692 [No Abstract] [Full Text] [Related]
12. 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]
13. Prenatal detection of the 17p11.2 duplication in Charcot-Marie-Tooth disease type 1A: necessity of a multidisciplinary approach for heterogeneous disorders. Bernard R; Boyer A; Nègre P; Malzac P; Latour P; Vandenberghe A; Philip N; Lévy N Eur J Hum Genet; 2002 May; 10(5):297-302. PubMed ID: 12082504 [TBL] [Abstract][Full Text] [Related]
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15. Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from France. Lucotte G; Berriche S; Bathelier C; Turpin JC; Jacob P; Paquet JM; Pluot M; Vandenberghe A Genet Couns; 1995; 6(4):355-60. PubMed ID: 8775423 [TBL] [Abstract][Full Text] [Related]
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17. Introduction to the Third International Symposium on Charcot-Marie-Tooth disorders. Shy ME; Kamholz J; Lovelace RE Ann N Y Acad Sci; 1999 Sep; 883():xiii-xviii. PubMed ID: 10586222 [No 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]
19. 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]