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.
188 related articles for article (PubMed ID: 2239969)
1. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969 [TBL] [Abstract][Full Text] [Related]
2. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17. Defesche JC; Hoogendijk JE; de Visser M; de Visser O; Bolhuis PA Neurology; 1990 Sep; 40(9):1450-3. PubMed ID: 2392234 [TBL] [Abstract][Full Text] [Related]
3. [Genetic linkage of the autosomal dominant form of Charcot-Marie-Tooth amyotrophy and 3 genetic markers on chromosome 1]. Ferák V; Kádasi L; Hrubisko M; Siváková D; Véghová E Cesk Neurol Neurochir; 1989 May; 52(3):200-7. PubMed ID: 2582521 [TBL] [Abstract][Full Text] [Related]
4. Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17. Middleton-Price HR; Harding AE; Monteiro C; Berciano J; Malcolm S Am J Hum Genet; 1990 Jan; 46(1):92-4. PubMed ID: 2294757 [TBL] [Abstract][Full Text] [Related]
5. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17. Vance JM; Nicholson GA; Yamaoka LH; Stajich J; Stewart CS; Speer MC; Hung WY; Roses AD; Barker D; Pericak-Vance MA Exp Neurol; 1989 May; 104(2):186-9. PubMed ID: 2707366 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I). Raeymaekers P; Timmerman V; De Jonghe P; Swerts L; Gheuens J; Martin JJ; Muylle L; De Winter G; Vandenberghe A; Van Broeckhoven C Am J Hum Genet; 1989 Dec; 45(6):953-8. PubMed ID: 2589322 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17. Patel PI; Franco B; Garcia C; Slaugenhaupt SA; Nakamura Y; Ledbetter DH; Chakravarti A; Lupski JR Am J Hum Genet; 1990 Apr; 46(4):801-9. PubMed ID: 2316525 [TBL] [Abstract][Full Text] [Related]
10. Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17. McAlpine PJ; Feasby TE; Hahn AF; Komarnicki L; James S; Guy C; Dixon M; Qayyum S; Wright J; Coopland G Genomics; 1990 Jul; 7(3):408-15. PubMed ID: 2365358 [TBL] [Abstract][Full Text] [Related]
11. Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree. Timmerman V; Raeymaekers P; Nelis E; De Jonghe P; Muylle L; Ceuterick C; Martin JJ; Van Broeckhoven C J Neurol Sci; 1992 May; 109(1):41-8. PubMed ID: 1517763 [TBL] [Abstract][Full Text] [Related]
13. 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]
15. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies]. Sevilla T Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities. Loprest LJ; Pericak-Vance MA; Stajich J; Gaskell PC; Lucas AM; Lennon F; Yamaoka LH; Roses AD; Vance JM Neurology; 1992 Mar; 42(3 Pt 1):597-601. PubMed ID: 1549221 [TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease. Hentati A; Lamy C; Melki J; Zuber M; Munnich A; de Recondo J Genomics; 1992 Jan; 12(1):155-7. PubMed ID: 1733853 [TBL] [Abstract][Full Text] [Related]
19. Exclusion analysis of Charcot-Marie-Tooth neuropathy (CMT1) with chromosome 1p markers. Raeymaekers P; De Jonghe P; Swerts L; De Winter G; Gheuens J; Martin JJ; Vandenberghe A; Van Broeckhoven C Cytogenet Cell Genet; 1989; 50(2-3):178-80. PubMed ID: 2570676 [TBL] [Abstract][Full Text] [Related]
20. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Ben Othmane K; Middleton LT; Loprest LJ; Wilkinson KM; Lennon F; Rozear MP; Stajich JM; Gaskell PC; Roses AD; Pericak-Vance MA Genomics; 1993 Aug; 17(2):370-5. PubMed ID: 8406488 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]