Similar articles for PMID: 2316525

Year	Number of Results
1926	1
1980	1
1982	2
1983	1
1985	1
1986	1
1987	6
1988	9
1989	17
1990	11
1991	12
1992	17
1993	7
1994	13
1995	10
1996	9
1997	6
1998	3
1999	7
2000	6
2001	8
2002	1
2003	1
2004	3
2006	1
2008	2
2012	1
2013	1
2024	0

1

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. Patel PI, et al. Am J Hum Genet. 1990 Apr;46(4):801-9. Am J Hum Genet. 1990. PMID: 2316525 Free PMC article.

2

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, et al. McAlpine PJ, et al. Genomics. 1990 Jul;7(3):408-15. doi: 10.1016/0888-7543(90)90175-t. Genomics. 1990. PMID: 2365358

3

Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.

Patel PI, Garcia C, Montes de Oca-Luna R, Malamut RI, Franco B, Slaugenhaupt S, Chakravarti A, Lupski JR. Patel PI, et al. Am J Hum Genet. 1990 Dec;47(6):926-34. Am J Hum Genet. 1990. PMID: 1978559 Free PMC article.

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. Middleton-Price HR, et al. Am J Hum Genet. 1990 Jan;46(1):92-4. Am J Hum Genet. 1990. PMID: 2294757 Free PMC article.

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. Vance JM, et al. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366

6

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. Sambuughin N, et al. J Neurol Sci. 1998 Nov 26;161(1):23-8. doi: 10.1016/s0022-510x(98)00264-0. J Neurol Sci. 1998. PMID: 9879677

7

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. Chance PF, et al. Am J Hum Genet. 1990 Dec;47(6):915-25. Am J Hum Genet. 1990. PMID: 2239969 Free PMC article.

8

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. Raeymaekers P, et al. Am J Hum Genet. 1989 Dec;45(6):953-8. Am J Hum Genet. 1989. PMID: 2589322 Free PMC article.

9

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. Timmerman V, et al. Am J Hum Genet. 1990 Oct;47(4):680-5. Am J Hum Genet. 1990. PMID: 2220808 Free PMC article.

10

Linkage in a family with X-linked Charcot-Marie-Tooth disease.

Haites N, Fairweather N, Clark C, Kelly KF, Simpson S, Johnston AW. Haites N, et al. Clin Genet. 1989 Jun;35(6):399-403. doi: 10.1111/j.1399-0004.1989.tb02964.x. Clin Genet. 1989. PMID: 2567643

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