136 related articles for article (PubMed ID: 8001963)
21. Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer.
Holmberg E; Rozell BL; Toftgård R
Br J Cancer; 1996 Jul; 74(2):246-50. PubMed ID: 8688329
[TBL] [Abstract][Full Text] [Related]
22. NBCCS secondary to an interstitial chromosome 9q deletion.
Haniffa MA; Leech SN; Lynch SA; Simpson NB
Clin Exp Dermatol; 2004 Sep; 29(5):542-4. PubMed ID: 15347344
[TBL] [Abstract][Full Text] [Related]
23. Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.
Edery P; Manach Y; Le Merrer M; Till M; Vignal A; Lyonnet S; Munnich A
Am J Med Genet; 1994 Aug; 52(2):174-7. PubMed ID: 7802004
[TBL] [Abstract][Full Text] [Related]
24. Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas.
Shanley SM; Dawkins H; Wainwright BJ; Wicking C; Heenan P; Eldon M; Searle J; Chenevix-Trench G
Hum Mol Genet; 1995 Jan; 4(1):129-33. PubMed ID: 7711724
[TBL] [Abstract][Full Text] [Related]
25. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
Vortmeyer AO; Stavrou T; Selby D; Li G; Weil RJ; Park WS; Moon YW; Chandra R; Goldstein AM; Zhuang Z
Cancer; 1999 Jun; 85(12):2662-7. PubMed ID: 10375116
[TBL] [Abstract][Full Text] [Related]
26. Odontogenic keratocyst and uterus bicornis in nevoid basal cell carcinoma syndrome: case report and literature review.
Ramaglia L; Morgese F; Pighetti M; Saviano R
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Aug; 102(2):217-9. PubMed ID: 16876065
[TBL] [Abstract][Full Text] [Related]
27. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF
Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3.
Chidambaram A; Gailani M; Gerrard B; Stewart C; Goldstein A; Chumakov I; Bale AE; Dean M
Genes Chromosomes Cancer; 1997 Mar; 18(3):212-8. PubMed ID: 9071574
[TBL] [Abstract][Full Text] [Related]
31. Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q.
Compton JG; Goldstein AM; Turner M; Bale AE; Kearns KS; McBride OW; Bale SJ
J Invest Dermatol; 1994 Aug; 103(2):178-81. PubMed ID: 8040607
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees.
Camp NJ; Farnham JM; Cannon-Albright LA
Cancer Res; 2006 Oct; 66(20):10205-12. PubMed ID: 17047086
[TBL] [Abstract][Full Text] [Related]
34. A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.
Jain PK; Lalwani AK; Li XC; Singleton TL; Smith TN; Chen A; Deshmukh D; Verma IC; Smith RJ; Wilcox ER
Genomics; 1998 Jun; 50(2):290-2. PubMed ID: 9653658
[TBL] [Abstract][Full Text] [Related]
35. The Gorlin syndrome gene: a tumor suppressor active in basal cell carcinogenesis and embryonic development.
Bale AE; Gailani MR; Leffell DJ
Proc Assoc Am Physicians; 1995 Jul; 107(2):253-7. PubMed ID: 8624861
[No Abstract] [Full Text] [Related]
36. Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.
Wang Y; Treat K; Schroer RJ; O'Brien JE; Stevenson RE; Schwartz CE
Am J Med Genet; 1994 Jun; 51(2):169-75. PubMed ID: 8092198
[TBL] [Abstract][Full Text] [Related]
37. High-resolution genetic mapping of the cartilage-hair hypoplasia (CHH) gene in Amish and Finnish families.
Sulisalo T; Francomano CA; Sistonen P; Maher JF; McKusick VA; de la Chapelle A; Kaitila I
Genomics; 1994 Apr; 20(3):347-53. PubMed ID: 8034306
[TBL] [Abstract][Full Text] [Related]
38. [Nevoid basal cell carcinoma syndrome].
Takata M
Nihon Rinsho; 2000 Jul; 58(7):1376-80. PubMed ID: 10921308
[TBL] [Abstract][Full Text] [Related]
39. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.
Hahn H; Wicking C; Zaphiropoulous PG; Gailani MR; Shanley S; Chidambaram A; Vorechovsky I; Holmberg E; Unden AB; Gillies S; Negus K; Smyth I; Pressman C; Leffell DJ; Gerrard B; Goldstein AM; Dean M; Toftgard R; Chenevix-Trench G; Wainwright B; Bale AE
Cell; 1996 Jun; 85(6):841-51. PubMed ID: 8681379
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]