472 related articles for article (PubMed ID: 8291533)
1. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
Ellison KA; Roth EJ; McCabe ER; Chinault AC; Zoghbi HY
Am J Med Genet; 1993 Nov; 47(7):1124-34. PubMed ID: 8291533
[TBL] [Abstract][Full Text] [Related]
2. Yeast artificial chromosome cloning of 3.2 megabases within chromosomal band 11q24 closely linking c-ets 1 and Fli-1 and encompassing the Ewing sarcoma breakpoint.
Selleri L; Giovannini M; Hermanson GG; Romo A; Quackenbush J; Penny L; Khristich JV; Evans GA
Genomics; 1994 Jul; 22(1):137-47. PubMed ID: 7959760
[TBL] [Abstract][Full Text] [Related]
3. Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.
Negrini M; Sabbioni S; Ohta M; Veronese ML; Rattan S; Junien C; Croce CM
Cancer Res; 1995 Jul; 55(13):2904-9. PubMed ID: 7796419
[TBL] [Abstract][Full Text] [Related]
4. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
Lanyi A; Li B; Li S; Talmadge CB; Brichacek B; Davis JR; Kozel BA; Trask B; van den Engh G; Uzvolgyi E; Stanbridge EJ; Nelson DL; Chinault C; Heslop H; Gross TG; Seemayer TA; Klein G; Purtilo DT; Sumegi J
Genomics; 1997 Jan; 39(1):55-65. PubMed ID: 9027486
[TBL] [Abstract][Full Text] [Related]
5. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
Forbes SA; Brennan L; Richardson M; Coffey A; Cole CG; Gregory SG; Bentley DR; Mumm S; Moore GE; Stanier P
Genomics; 1996 Jan; 31(1):36-43. PubMed ID: 8808277
[TBL] [Abstract][Full Text] [Related]
6. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
Francis F; Benham F; See CG; Fox M; Ishikawa-Brush Y; Monaco AP; Weiss B; Rappold G; Hamvas RM; Lehrach H
Genomics; 1994 Mar; 20(1):75-83. PubMed ID: 8020959
[TBL] [Abstract][Full Text] [Related]
7. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L
Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085
[TBL] [Abstract][Full Text] [Related]
8. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG
Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
[TBL] [Abstract][Full Text] [Related]
9. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
Wedemeyer N; Lengeling A; Ronsiek M; Korthaus D; Baer K; Wuttke M; Jockusch H
Genomics; 1996 Mar; 32(3):447-54. PubMed ID: 8838809
[TBL] [Abstract][Full Text] [Related]
10. The generation and regional localization of 303 new chromosome 5 sequence-tagged sites.
Grady DL; Robinson DL; Gersh M; Nickerson E; McPherson J; Wasmuth JJ; Overhauser J; Deaven LL; Moyzis RK
Genomics; 1996 Feb; 32(1):91-6. PubMed ID: 8786125
[TBL] [Abstract][Full Text] [Related]
11. A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.
Lee WC; Ferrero GB; Chinault AC; Yen PH; Ballabio A
Genomics; 1993 Oct; 18(1):1-6. PubMed ID: 8276392
[TBL] [Abstract][Full Text] [Related]
12. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.
Wilke CM; Guo SW; Hall BK; Boldog F; Gemmill RM; Chandrasekharappa SC; Barcroft CL; Drabkin HA; Glover TW
Genomics; 1994 Jul; 22(2):319-26. PubMed ID: 7806217
[TBL] [Abstract][Full Text] [Related]
13. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
Gorski JL; Bialecki MD; McDonald MT; Massa HF; Trask BJ; Burright EN
Genomics; 1996 Jul; 35(2):338-45. PubMed ID: 8661147
[TBL] [Abstract][Full Text] [Related]
14. Construction of a yeast artificial chromosome contig encompassing the human acidic fibroblast growth factor (FGF1) gene: toward the cloning of the ANLL/MDS tumor-suppressor gene.
Chiu IM; Gilmore EC; Liu Y; Payson RA
Genomics; 1994 Feb; 19(3):552-60. PubMed ID: 7514571
[TBL] [Abstract][Full Text] [Related]
15. A de novo X;3 translocation in Rett syndrome.
Zoghbi HY; Ledbetter DH; Schultz R; Percy AK; Glaze DG
Am J Med Genet; 1990 Jan; 35(1):148-51. PubMed ID: 2301468
[TBL] [Abstract][Full Text] [Related]
16. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
Paradee W; Wilke CM; Wang L; Shridhar R; Mullins CM; Hoge A; Glover TW; Smith DI
Genomics; 1996 Jul; 35(1):87-93. PubMed ID: 8661108
[TBL] [Abstract][Full Text] [Related]
17. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
Wilgenbus KK; Seranski P; Brown A; Leuchs B; Mincheva A; Lichter P; Poustka A
Genomics; 1997 May; 42(1):1-10. PubMed ID: 9177769
[TBL] [Abstract][Full Text] [Related]
18. A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255.
Boycott KM; Halley GR; Schlessinger D; Bech-Hansen NT
Genomics; 1996 May; 33(3):488-97. PubMed ID: 8661008
[TBL] [Abstract][Full Text] [Related]
19. Refinement of a translocation breakpoint associated with blepharophimosis-ptosis-epicanthus inversus syndrome to a 280-kb interval at chromosome 3q23.
Toomes C; Dixon MJ
Genomics; 1998 Nov; 53(3):308-14. PubMed ID: 9799597
[TBL] [Abstract][Full Text] [Related]
20. Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1.
Knight JC; Grimaldi G; Thiesen HJ; Bech-Hansen NT; Fletcher CD; Coleman MP
Genomics; 1994 May; 21(1):180-7. PubMed ID: 8088786
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
