74 related articles for article (PubMed ID: 7835901)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
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. Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.
Shimkets R; Gailani MR; Siu VM; Yang-Feng T; Pressman CL; Levanat S; Goldstein A; Dean M; Bale AE
Am J Hum Genet; 1996 Aug; 59(2):417-22. PubMed ID: 8755929
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.
Biancalana V; Trivier E; Weber C; Weissenbach J; Rowe PS; O'Riordan JL; Partington MW; Heyberger S; Oudet C; Hanauer A
Genomics; 1994 Aug; 22(3):617-25. PubMed ID: 8001973
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.
Gibson RA; Ford D; Jansen S; Savoia A; Havenga C; Milner RD; de Ravel TJ; Cohn RJ; Ball SE; Roberts I
J Med Genet; 1994 Nov; 31(11):868-71. PubMed ID: 7853372
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. High-resolution recombinational map of mouse chromosome 16.
Reeves RH; Rue EE; Citron MP; Cabin DE
Genomics; 1997 Jul; 43(2):202-8. PubMed ID: 9244437
[TBL] [Abstract][Full Text] [Related]
14. An EST and STS-based YAC contig map of human chromosome 9q22.3.
Lench NJ; Telford EA; Andersen SE; Moynihan TP; Robinson PA; Markham AF
Genomics; 1996 Dec; 38(2):199-205. PubMed ID: 8954802
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Fructose-1,6-bisphosphatase: genetic and physical mapping to human chromosome 9q22.3 and evaluation in non-insulin-dependent diabetes mellitus.
Rothschild CB; Freedman BI; Hodge R; Rao PN; Pettenati MJ; Anderson RA; Akots G; Qadri A; Roh B; Fajans SS
Genomics; 1995 Sep; 29(1):187-94. PubMed ID: 8530070
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes.
Richards FM; Goudie DR; Cooper WN; Jene Q; Barroso I; Wicking C; Wainwright BJ; Ferguson-Smith MA
Hum Genet; 1997 Dec; 101(3):317-22. PubMed ID: 9439661
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
