126 related articles for article (PubMed ID: 12438263)
1. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.
Maris JM; Weiss MJ; Mosse Y; Hii G; Guo C; White PS; Hogarty MD; Mirensky T; Brodeur GM; Rebbeck TR; Urbanek M; Shusterman S
Cancer Res; 2002 Nov; 62(22):6651-8. PubMed ID: 12438263
[TBL] [Abstract][Full Text] [Related]
2. Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13.
Weiss MJ; Guo C; Shusterman S; Hii G; Mirensky TL; White PS; Hogarty MD; Rebbeck TR; Teare D; Urbanek M; Brodeur GM; Maris JM
Med Pediatr Oncol; 2000 Dec; 35(6):526-30. PubMed ID: 11107108
[TBL] [Abstract][Full Text] [Related]
3. Genetic predisposition to familial neuroblastoma: identification of two novel genomic regions at 2p and 12p.
Longo L; Panza E; Schena F; Seri M; Devoto M; Romeo G; Bini C; Pappalardo G; Tonini GP; Perri P
Hum Hered; 2007; 63(3-4):205-11. PubMed ID: 17317969
[TBL] [Abstract][Full Text] [Related]
4. Weak linkage at 4p16 to predisposition for human neuroblastoma.
Perri P; Longo L; Cusano R; McConville CM; Rees SA; Devoto M; Conte M; Ferrara GB; Seri M; Romeo G; Tonini GP
Oncogene; 2002 Nov; 21(54):8356-60. PubMed ID: 12447700
[TBL] [Abstract][Full Text] [Related]
5. Familial predisposition to neuroblastoma does not map to chromosome band 1p36.
Maris JM; Kyemba SM; Rebbeck TR; White PS; Sulman EP; Jensen SJ; Allen C; Biegel JA; Yanofsky RA; Feldman GL; Brodeur GM
Cancer Res; 1996 Aug; 56(15):3421-5. PubMed ID: 8758905
[TBL] [Abstract][Full Text] [Related]
6. Novel pheochromocytoma susceptibility loci identified by integrative genomics.
Dahia PL; Hao K; Rogus J; Colin C; Pujana MA; Ross K; Magoffin D; Aronin N; Cascon A; Hayashida CY; Li C; Toledo SP; Stiles CD;
Cancer Res; 2005 Nov; 65(21):9651-8. PubMed ID: 16266984
[TBL] [Abstract][Full Text] [Related]
7. Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.
Weber YG; Berger A; Bebek N; Maier S; Karafyllakes S; Meyer N; Fukuyama Y; Halbach A; Hikel C; Kurlemann G; Neubauer B; Osawa M; Püst B; Rating D; Saito K; Stephani U; Tauer U; Lehmann-Horn F; Jurkat-Rott K; Lerche H
Epilepsia; 2004 Jun; 45(6):601-9. PubMed ID: 15144424
[TBL] [Abstract][Full Text] [Related]
8. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
[TBL] [Abstract][Full Text] [Related]
9. Analysis of loss of heterozygosity at 16p12-p13 (familial neuroblastoma locus) in 470 neuroblastomas including both sporadic and mass screening tumors.
Furuta S; Ohira M; Machida T; Hamano S; Nakagawara A
Med Pediatr Oncol; 2000 Dec; 35(6):531-3. PubMed ID: 11107109
[TBL] [Abstract][Full Text] [Related]
10. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors.
McDonald JM; Douglass EC; Fisher R; Geiser CF; Krill CE; Strong LC; Virshup D; Huff V
Cancer Res; 1998 Apr; 58(7):1387-90. PubMed ID: 9537236
[TBL] [Abstract][Full Text] [Related]
11. Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis.
Krona C; Carén H; Sjöberg RM; Sandstedt B; Laureys G; Kogner P; Martinsson T
Int J Oncol; 2008 Mar; 32(3):575-83. PubMed ID: 18292934
[TBL] [Abstract][Full Text] [Related]
12. Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.
Bourdeaut F; Trochet D; Janoueix-Lerosey I; Ribeiro A; Deville A; Coz C; Michiels JF; Lyonnet S; Amiel J; Delattre O
Cancer Lett; 2005 Oct; 228(1-2):51-8. PubMed ID: 15949893
[TBL] [Abstract][Full Text] [Related]
13. Finer linkage mapping of primary osteoarthritis susceptibility loci on chromosomes 4 and 16 in families with affected women.
Forster T; Chapman K; Marcelline L; Mustafa Z; Southam L; Loughlin J
Arthritis Rheum; 2004 Jan; 50(1):98-102. PubMed ID: 14730605
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant multiple syringomas linked to chromosome 16q22.
Wu WM; Lee YS
Br J Dermatol; 2010 May; 162(5):1083-7. PubMed ID: 20132207
[TBL] [Abstract][Full Text] [Related]
15. Genetics and genomics of neuroblastoma.
Capasso M; Diskin SJ
Cancer Treat Res; 2010; 155():65-84. PubMed ID: 20517688
[TBL] [Abstract][Full Text] [Related]
16. Refinement of the chromosome 16 locus for benign familial infantile convulsions.
Callenbach PM; van den Boogerd EH; de Coo RF; ten Houten R; Oosterwijk JC; Hageman G; Frants RR; Brouwer OF; van den Maagdenberg AM
Clin Genet; 2005 Jun; 67(6):517-25. PubMed ID: 15857419
[TBL] [Abstract][Full Text] [Related]
17. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C
Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746
[TBL] [Abstract][Full Text] [Related]
18. Evidence for multiple loci from a genome scan of autism kindreds.
Schellenberg GD; Dawson G; Sung YJ; Estes A; Munson J; Rosenthal E; Rothstein J; Flodman P; Smith M; Coon H; Leong L; Yu CE; Stodgell C; Rodier PM; Spence MA; Minshew N; McMahon WM; Wijsman EM
Mol Psychiatry; 2006 Nov; 11(11):1049-60, 979. PubMed ID: 16880825
[TBL] [Abstract][Full Text] [Related]
19. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L
Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
