These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 8012356)

  • 1. Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.
    Bonifas JM; Bare JW; Kerschmann RL; Master SP; Epstein EH
    Hum Mol Genet; 1994 Mar; 3(3):447-8. PubMed ID: 8012356
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts.
    Lench NJ; High AS; Markham AF; Hume WJ; Robinson PA
    Eur J Cancer B Oral Oncol; 1996 May; 32B(3):202-6. PubMed ID: 8762878
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.
    Boonen SE; Stahl D; Kreiborg S; Rosenberg T; Kalscheuer V; Larsen LA; Tommerup N; Brøndum-Nielsen K; Tümer Z
    Am J Med Genet A; 2005 Jan; 132A(3):324-8. PubMed ID: 15690381
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.
    Olivieri C; Maraschio P; Caselli D; Martini C; Beluffi G; Maserati E; Danesino C
    Eur J Pediatr; 2003 Feb; 162(2):100-3. PubMed ID: 12548386
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Nevoid basal cell carcinoma syndrome.
    Bale AE; Gailani MR; Leffell DJ
    J Invest Dermatol; 1994 Nov; 103(5 Suppl):126S-130S. PubMed ID: 7963674
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.
    Chen CP; Lin SP; Wang TH; Chen YJ; Chen M; Wang W
    Prenat Diagn; 2006 Aug; 26(8):725-9. PubMed ID: 16927391
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [From gene to disease: basal cell naevus syndrome].
    de Meij TG; Baars MJ; Gille JJ; Hack WW; Haasnoot K; van Hagen JM
    Ned Tijdschr Geneeskd; 2005 Jan; 149(2):78-81. PubMed ID: 15688838
    [TBL] [Abstract][Full Text] [Related]  

  • 11. No evidence of mutation in the human PTC gene, responsible for nevoid basal cell carcinoma syndrome, in human primary squamous cell carcinomas of the esophagus and lung.
    Suzuki K; Daigo Y; Fukuda S; Tokino T; Isomura M; Isono K; Wainwright B; Nakamura Y
    Jpn J Cancer Res; 1997 Mar; 88(3):225-8. PubMed ID: 9140104
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [A nevoid basal cell carcinoma syndrome with chromosomal aberration].
    Sasaki K; Yoshimoto T; Nakao T; Minagawa K; Takahashi Y; Watanabe Y; Tanabe C
    No To Hattatsu; 2000 Jan; 32(1):49-55. PubMed ID: 10655752
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Gorlin syndrome patient with large deletion in 9q22.32-q22.33 detected by quantitative multiplex fluorescent PCR.
    Musani V; Cretnik M; Situm M; Basta-Juzbasic A; Levanat S
    Dermatology; 2009; 219(2):111-8. PubMed ID: 19439922
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9.
    Gailani MR; Bale SJ; Leffell DJ; DiGiovanna JJ; Peck GL; Poliak S; Drum MA; Pastakia B; McBride OW; Kase R
    Cell; 1992 Apr; 69(1):111-7. PubMed ID: 1348213
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 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. Destructive basal cell carcinoma in a patient with basal cell nevus syndrome and an interstitial deletion of chromosome 9q22.
    Mosterd K; Sommer A; van Marion A; Lacko M; Herbergs J; de Bondt BJ; van Steensel MA; Kelleners-Smeets NW
    Dermatol Surg; 2009 Dec; 35(12):2051-3. PubMed ID: 20050151
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.