212 related articles for article (PubMed ID: 2020294)
21. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
Hedera P; Blair MA; Andermann E; Andermann F; D'Agostino D; Taylor KA; Chahine L; Pandolfo M; Bradford Y; Haines JL; Abou-Khalil B
Neurology; 2007 Jun; 68(24):2107-12. PubMed ID: 17377072
[TBL] [Abstract][Full Text] [Related]
22. Gene linkage in familial amyotrophic lateral sclerosis: a progress report.
Brown RH; Horvitz HR; Rouleau GA; McKenna-Yasek D; Beard C; Sapp P; Haines JL; Gusella JF; Figlewicz DA
Adv Neurol; 1991; 56():215-26. PubMed ID: 1853758
[No Abstract] [Full Text] [Related]
23. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
[TBL] [Abstract][Full Text] [Related]
24. Molecular genetics of familial amyotrophic lateral sclerosis.
Siddique T
Adv Neurol; 1991; 56():227-31. PubMed ID: 1853759
[No Abstract] [Full Text] [Related]
25. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.
Justice CM; Miller NH; Marosy B; Zhang J; Wilson AF
Spine (Phila Pa 1976); 2003 Mar; 28(6):589-94. PubMed ID: 12642767
[TBL] [Abstract][Full Text] [Related]
26. Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
Leppert M; Anderson VE; Quattlebaum T; Stauffer D; O'Connell P; Nakamura Y; Lalouel JM; White R
Nature; 1989 Feb; 337(6208):647-8. PubMed ID: 2918897
[TBL] [Abstract][Full Text] [Related]
27. Genetic basis of familial amyotrophic lateral sclerosis.
N Engl J Med; 1991 Nov; 325(19):1382-3. PubMed ID: 1922244
[No Abstract] [Full Text] [Related]
28. Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21.
Figlewicz DA; McInnis MG; Goto J; Haines JL; Warren AC; Krizus A; Khodr N; Brown RH; McKenna-Yasek D; Antonarakis SE
J Neurol Sci; 1994 Jul; 124 Suppl():90-5. PubMed ID: 7807155
[TBL] [Abstract][Full Text] [Related]
29. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.
Chance PF; Rabin BA; Ryan SG; Ding Y; Scavina M; Crain B; Griffin JW; Cornblath DR
Am J Hum Genet; 1998 Mar; 62(3):633-40. PubMed ID: 9497266
[TBL] [Abstract][Full Text] [Related]
30. The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis.
Goto J; Figlewicz DA; Haines JL; Brown RH; Khodr N; Rouleau GA
Neuromuscul Disord; 1993 Mar; 3(2):157-60. PubMed ID: 8358240
[TBL] [Abstract][Full Text] [Related]
31. Linkage analysis in familial amyotrophic lateral sclerosis.
Siddique T; Pericak-Vance MA; Brooks BR; Roos RP; Hung WY; Antel JP; Munsat TL; Phillips K; Warner K; Speer M
Neurology; 1989 Jul; 39(7):919-25. PubMed ID: 2739919
[TBL] [Abstract][Full Text] [Related]
32. Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.
King A; Houlden H; Hardy J; Lane R; Chancellor A; de Belleroche J
J Med Genet; 1993 Apr; 30(4):318. PubMed ID: 8487280
[TBL] [Abstract][Full Text] [Related]
33. More than one locus for familial amyotrophic lateral sclerosis: absence of linkage to the SMA locus.
King AW; Orrell RW; Lane R; de Belleroche JS
Biochem Soc Trans; 1994 May; 22(2):149S. PubMed ID: 7958219
[No Abstract] [Full Text] [Related]
34. A first step toward a molecular genetic analysis of amyotrophic lateral sclerosis.
Conneally PM
N Engl J Med; 1991 May; 324(20):1430-2. PubMed ID: 2020300
[No Abstract] [Full Text] [Related]
35. A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.
Abalkhail H; Mitchell J; Habgood J; Orrell R; de Belleroche J
Am J Hum Genet; 2003 Aug; 73(2):383-9. PubMed ID: 12830400
[TBL] [Abstract][Full Text] [Related]
36. Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.
Hosler BA; Siddique T; Sapp PC; Sailor W; Huang MC; Hossain A; Daube JR; Nance M; Fan C; Kaplan J; Hung WY; McKenna-Yasek D; Haines JL; Pericak-Vance MA; Horvitz HR; Brown RH
JAMA; 2000 Oct; 284(13):1664-9. PubMed ID: 11015796
[TBL] [Abstract][Full Text] [Related]
37. Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
Lehesjoki AE; Koskiniemi M; Sistonen P; Miao J; Hästbacka J; Norio R; de la Chapelle A
Proc Natl Acad Sci U S A; 1991 May; 88(9):3696-9. PubMed ID: 1673790
[TBL] [Abstract][Full Text] [Related]
38. Odds and SODS.
Nat Genet; 1993 Apr; 3(4):275-6. PubMed ID: 7981742
[No Abstract] [Full Text] [Related]
39. The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis.
Eubanks JH; Puranam RS; Kleckner NW; Bettler B; Heinemann SF; McNamara JO
Proc Natl Acad Sci U S A; 1993 Jan; 90(1):178-82. PubMed ID: 8419920
[TBL] [Abstract][Full Text] [Related]
40. Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.
Gregor P; Reeves RH; Jabs EW; Yang X; Dackowski W; Rochelle JM; Brown RH; Haines JL; O'Hara BF; Uhl GR
Proc Natl Acad Sci U S A; 1993 Apr; 90(7):3053-7. PubMed ID: 8464923
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
