136 related articles for article (PubMed ID: 8001963)
1. Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome.
Wicking C; Berkman J; Wainwright B; Chenevix-Trench G
Genomics; 1994 Aug; 22(3):505-11. PubMed ID: 8001963
[TBL] [Abstract][Full Text] [Related]
2. Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.
Chenevix-Trench G; Wicking C; Berkman J; Sharpe H; Hockey A; Haan E; Oley C; Ravine D; Turner A; Goldgar D
Am J Hum Genet; 1993 Sep; 53(3):760-7. PubMed ID: 8352281
[TBL] [Abstract][Full Text] [Related]
3. Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3.
Farndon PA; Morris DJ; Hardy C; McConville CM; Weissenbach J; Kilpatrick MW; Reis A
Genomics; 1994 Sep; 23(2):486-9. PubMed ID: 7835901
[TBL] [Abstract][Full Text] [Related]
4. A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9q.
Morris DJ; Reis A
Genomics; 1994 Sep; 23(1):23-9. PubMed ID: 7829076
[TBL] [Abstract][Full Text] [Related]
5. Physical mapping of the 5 Mb D9S196-D9S180 interval harboring the basal cell nevus syndrome gene and localization of six genes in this region.
Xie J; Quinn A; Zhang X; Bare J; Rothman A; Collins C; Cutone S; Rutter M; McCormick MK; Epstein E
Genes Chromosomes Cancer; 1997 Apr; 18(4):305-9. PubMed ID: 9087571
[TBL] [Abstract][Full Text] [Related]
6. Localization of the gene for the nevoid basal cell carcinoma syndrome.
Goldstein AM; Stewart C; Bale AE; Bale SJ; Dean M
Am J Hum Genet; 1994 May; 54(5):765-73. PubMed ID: 7909984
[TBL] [Abstract][Full Text] [Related]
7. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
Simoneau AR; Spruck CH; Gonzalez-Zulueta M; Gonzalgo ML; Chan MF; Tsai YC; Dean M; Steven K; Horn T; Jones PA
Cancer Res; 1996 Nov; 56(21):5039-43. PubMed ID: 8895761
[TBL] [Abstract][Full Text] [Related]
8. Genetic instability of microsatellite markers in region q22.3-q31 of chromosome 9 in skin squamous cell carcinomas.
Zaphiropoulos PG; Söderkvist P; Hedblad MA; Toftgård R
Biochem Biophys Res Commun; 1994 Jun; 201(3):1495-501. PubMed ID: 8024595
[TBL] [Abstract][Full Text] [Related]
9. Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas.
Schofield D; West DC; Anthony DC; Marshal R; Sklar J
Am J Pathol; 1995 Feb; 146(2):472-80. PubMed ID: 7856756
[TBL] [Abstract][Full Text] [Related]
10. Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.
Yamamoto K; Yoshihashi H; Furuya N; Adachi M; Ito S; Tanaka Y; Masuno M; Chiyo H; Kurosawa K
Congenit Anom (Kyoto); 2009 Mar; 49(1):8-14. PubMed ID: 19243411
[TBL] [Abstract][Full Text] [Related]
11. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
Vorechovský I; Tingby O; Hartman M; Strömberg B; Nister M; Collins VP; Toftgård R
Oncogene; 1997 Jul; 15(3):361-6. PubMed ID: 9233770
[TBL] [Abstract][Full Text] [Related]
12. A two-hit model for developmental defects in Gorlin syndrome.
Levanat S; Gorlin RJ; Fallet S; Johnson DR; Fantasia JE; Bale AE
Nat Genet; 1996 Jan; 12(1):85-7. PubMed ID: 8528259
[No Abstract] [Full Text] [Related]
13. Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q.
Undén AB; Ståhle-Bäckdahl M; Holmberg E; Larsson C; Toftgård R
Acta Derm Venereol; 1997 Jan; 77(1):4-9. PubMed ID: 9059667
[TBL] [Abstract][Full Text] [Related]
14. Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.
Levanat S; Chidambaram A; Wicking C; Bray-Ward P; Pressman C; Toftgard R; Gailani MR; Myers JC; Wainwright B; Dean M; Bale AE
Cytogenet Cell Genet; 1997; 76(3-4):208-13. PubMed ID: 9186526
[TBL] [Abstract][Full Text] [Related]
15. Nevoid basal cell carcinoma syndrome: a review of the literature.
Manfredi M; Vescovi P; Bonanini M; Porter S
Int J Oral Maxillofac Surg; 2004 Mar; 33(2):117-24. PubMed ID: 15050066
[TBL] [Abstract][Full Text] [Related]
16. Variable expression of Gorlin syndrome may reflect complexity of the signalling pathway.
Levanat S; Mubrin MK; Crnić I; Situm M; Basta-Juzbasić A
Pflugers Arch; 2000; 439(3 Suppl):R31-3. PubMed ID: 10653132
[TBL] [Abstract][Full Text] [Related]
17. Nevoid basal cell carcinoma syndrome: review of 118 affected individuals.
Shanley S; Ratcliffe J; Hockey A; Haan E; Oley C; Ravine D; Martin N; Wicking C; Chenevix-Trench G
Am J Med Genet; 1994 Apr; 50(3):282-90. PubMed ID: 8042673
[TBL] [Abstract][Full Text] [Related]
18. Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site.
Bare JW; Lebo RV; Epstein EH
Cancer Res; 1992 Mar; 52(6):1494-8. PubMed ID: 1540957
[TBL] [Abstract][Full Text] [Related]
19. Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.
Goudie DR; Yuille MA; Leversha MA; Furlong RA; Carter NP; Lush MJ; Affara NA; Ferguson-Smith MA
Nat Genet; 1993 Feb; 3(2):165-9. PubMed ID: 8499949
[TBL] [Abstract][Full Text] [Related]
20. Location of gene for Gorlin syndrome.
Farndon PA; Del Mastro RG; Evans DG; Kilpatrick MW
Lancet; 1992 Mar; 339(8793):581-2. PubMed ID: 1347096
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]