166 related articles for article (PubMed ID: 11774073)
21. A gene for episodic ataxia/myokymia maps to chromosome 12p13.
Litt M; Kramer P; Browne D; Gancher S; Brunt ER; Root D; Phromchotikul T; Dubay CJ; Nutt J
Am J Hum Genet; 1994 Oct; 55(4):702-9. PubMed ID: 7942848
[TBL] [Abstract][Full Text] [Related]
22. A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.
Hand CK; Khoris J; Salachas F; Gros-Louis F; Lopes AA; Mayeux-Portas V; Brewer CG; Brown RH; Meininger V; Camu W; Rouleau GA
Am J Hum Genet; 2002 Jan; 70(1):251-6. PubMed ID: 11706389
[TBL] [Abstract][Full Text] [Related]
23. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
Hanein S; Dürr A; Ribai P; Forlani S; Leutenegger AL; Nelson I; Babron MC; Elleuch N; Depienne C; Charon C; Brice A; Stevanin G
Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
[TBL] [Abstract][Full Text] [Related]
24. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
Zu L; Figueroa KP; Grewal R; Pulst SM
Am J Hum Genet; 1999 Feb; 64(2):594-9. PubMed ID: 9973298
[TBL] [Abstract][Full Text] [Related]
25. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.
Greene CC; McMillan PM; Barker SE; Kurnool P; Lomax MI; Burmeister M; Lesperance MM
Am J Hum Genet; 2001 Jan; 68(1):254-60. PubMed ID: 11115382
[TBL] [Abstract][Full Text] [Related]
26. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
Desautels A; Turecki G; Montplaisir J; Sequeira A; Verner A; Rouleau GA
Am J Hum Genet; 2001 Dec; 69(6):1266-70. PubMed ID: 11704926
[TBL] [Abstract][Full Text] [Related]
27. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
Morlé L; Bozon M; Zech JC; Alloisio N; Raas-Rothschild A; Philippe C; Lambert JC; Godet J; Plauchu H; Edery P
Am J Hum Genet; 2000 Dec; 67(6):1592-7. PubMed ID: 11035633
[TBL] [Abstract][Full Text] [Related]
28. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
Gispert S; Santos N; Damen R; Voit T; Schulz J; Klockgether T; Orozco G; Kreuz F; Weissenbach J; Auburger G
Am J Hum Genet; 1995 Jan; 56(1):183-7. PubMed ID: 7825576
[TBL] [Abstract][Full Text] [Related]
29. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Waters MF; Fee D; Figueroa KP; Nolte D; Müller U; Advincula J; Coon H; Evidente VG; Pulst SM
Neurology; 2005 Oct; 65(7):1111-3. PubMed ID: 16135769
[TBL] [Abstract][Full Text] [Related]
30. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
Reid E; Dearlove AM; Whiteford ML; Rhodes M; Rubinsztein DC
Neurology; 1999 Nov; 53(8):1844-9. PubMed ID: 10563637
[TBL] [Abstract][Full Text] [Related]
31. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
Vazza G; Zortea M; Boaretto F; Micaglio GF; Sartori V; Mostacciuolo ML
Am J Hum Genet; 2000 Aug; 67(2):504-9. PubMed ID: 10877981
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan.
El-Shanti H; Daoud A; Sadoon AA; Leal SM; Chen S; Lee K; Spiegel R
Brain Dev; 2006 Jul; 28(6):353-7. PubMed ID: 16376507
[TBL] [Abstract][Full Text] [Related]
34. Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12.
Nechiporuk A; Lopes-Cendes I; Nechiporuk T; Starkman S; Andermann E; Rouleau GA; Weissenbach JS; Kort E; Pulst SM
Neurology; 1996 Jun; 46(6):1731-5. PubMed ID: 8649579
[TBL] [Abstract][Full Text] [Related]
35. Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31.
Evans JC; Frayling TM; Ellard S; Gutowski NJ
Hum Genet; 2000 Jun; 106(6):636-8. PubMed ID: 10942112
[TBL] [Abstract][Full Text] [Related]
36. A novel locus for autosomal recessive spastic ataxia on chromosome 17p.
Bouslam N; Bouhouche A; Benomar A; Hanein S; Klebe S; Azzedine H; Di Giandomenico S; Boland-Augé A; Santorelli FM; Durr A; Brice A; Yahyaoui M; Stevanin G
Hum Genet; 2007 May; 121(3-4):413-20. PubMed ID: 17273843
[TBL] [Abstract][Full Text] [Related]
37. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Brkanac Z; Bylenok L; Fernandez M; Matsushita M; Lipe H; Wolff J; Nochlin D; Raskind WH; Bird TD
Arch Neurol; 2002 Aug; 59(8):1291-5. PubMed ID: 12164726
[TBL] [Abstract][Full Text] [Related]
38. Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.
Xiong L; Labuda M; Li DS; Hudson TJ; Desbiens R; Patry G; Verret S; Langevin P; Mercho S; Seni MH; Scheffer I; Dubeau F; Berkovic SF; Andermann F; Andermann E; Pandolfo M
Am J Hum Genet; 1999 Dec; 65(6):1698-710. PubMed ID: 10577924
[TBL] [Abstract][Full Text] [Related]
39. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
Gispert S; Twells R; Orozco G; Brice A; Weber J; Heredero L; Scheufler K; Riley B; Allotey R; Nothers C
Nat Genet; 1993 Jul; 4(3):295-9. PubMed ID: 8358438
[TBL] [Abstract][Full Text] [Related]
40. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
Nürnberg G; Jacobi FK; Broghammer M; Becker C; Blin N; Nürnberg P; Stephani U; Pusch CM
Int J Mol Med; 2008 Apr; 21(4):429-38. PubMed ID: 18360688
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
