162 related articles for article (PubMed ID: 1684084)
41. Genetic and radiation-reduced somatic cell hybrid sublocalization of the human GSTP1 gene.
Smith CM; Bora PS; Bora NS; Jones C; Gerhard DS
Cytogenet Cell Genet; 1995; 71(3):235-9. PubMed ID: 7587384
[TBL] [Abstract][Full Text] [Related]
42. Putative tumor-suppressor gene on chromosome 11 is important in sporadic endocrine tumor formation.
Eubanks PJ; Sawicki MP; Samara GJ; Gatti R; Nakamura Y; Tsao D; Johnson C; Hurwitz M; Wan YJ; Passaro E
Am J Surg; 1994 Jan; 167(1):180-5. PubMed ID: 7906100
[TBL] [Abstract][Full Text] [Related]
43. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
[TBL] [Abstract][Full Text] [Related]
44. Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease.
Luo Y; Ceccherini I; Pasini B; Matera I; Bicocchi MP; Barone V; Bocciardi R; Kääriäinen H; Weber D; Devoto M
Hum Mol Genet; 1993 Nov; 2(11):1803-8. PubMed ID: 7904208
[TBL] [Abstract][Full Text] [Related]
45. Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1.
Röhme D; Sidén T; van der Maarel SM; Cremers FP; Tantravahi U; Marinoni JC; Ropers HH; Schwartz CE
Somat Cell Mol Genet; 1994 Jan; 20(1):1-10. PubMed ID: 8197472
[TBL] [Abstract][Full Text] [Related]
46. Regional assignment of a human DNA repair gene (XRCC5) to 2q35 by X-ray hybrid mapping.
Chen DJ; Marrone BL; Nguyen T; Stackhouse M; Zhao Y; Siciliano MJ
Genomics; 1994 May; 21(2):423-7. PubMed ID: 8088837
[TBL] [Abstract][Full Text] [Related]
47. Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping.
Mathew CG; Wakeling W; Jones E; Easton D; Fisher R; Strong C; Smith B; Chin K; Little P; Nakamura Y
Ann Hum Genet; 1990 May; 54(2):121-9. PubMed ID: 1974407
[TBL] [Abstract][Full Text] [Related]
48. A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus.
Rochelle JM; Watson ML; Oakey RJ; Seldin MF
Genomics; 1992 Sep; 14(1):26-31. PubMed ID: 1358795
[TBL] [Abstract][Full Text] [Related]
49. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.
Glaser T; Rose E; Morse H; Housman D; Jones C
Genomics; 1990 Jan; 6(1):48-64. PubMed ID: 2154397
[TBL] [Abstract][Full Text] [Related]
50. [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]
51. A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5q.
Loftus SK; Edwards SJ; Scherpbier-Heddema T; Buetow KH; Wasmuth JJ; Dixon MJ
Hum Mol Genet; 1993 Nov; 2(11):1785-92. PubMed ID: 8281138
[TBL] [Abstract][Full Text] [Related]
52. A 2.8 Mb YAC contig in 11q12-q13 localizes candidate genes for atopy: Fc epsilon RI beta and CD20.
Stafford AN; Rider SH; Hopkin JM; Cookson WO; Monaco AP
Hum Mol Genet; 1994 May; 3(5):779-85. PubMed ID: 7521709
[TBL] [Abstract][Full Text] [Related]
53. A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus.
Guru SC; Agarwal SK; Manickam P; Olufemi SE; Crabtree JS; Weisemann JM; Kester MB; Kim YS; Wang Y; Emmert-Buck MR; Liotta LA; Spiegel AM; Boguski MS; Roe BA; Collins FS; Marx SJ; Burns L; Chandrasekharappa SC
Genome Res; 1997 Jul; 7(7):725-35. PubMed ID: 9253601
[TBL] [Abstract][Full Text] [Related]
54. Distinct breakpoints in band 11q23 of the t(4;11) and t(11;14) associated with leukocyte malignancy.
Radice P; Tunnacliffe A
Genes Chromosomes Cancer; 1992 Jul; 5(1):50-6. PubMed ID: 1384662
[TBL] [Abstract][Full Text] [Related]
55. A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5.
Warrington JA; Bailey SK; Armstrong E; Aprelikova O; Alitalo K; Dolganov GM; Wilcox AS; Sikela JM; Wolfe SF; Lovett M
Genomics; 1992 Jul; 13(3):803-8. PubMed ID: 1322355
[TBL] [Abstract][Full Text] [Related]
56. A 1.5-megabase yeast artificial chromosome contig from human chromosome 10q11.2 connecting three genetic loci (RET, D10S94, and D10S102) closely linked to the MEN2A locus.
Lairmore TC; Dou S; Howe JR; Chi D; Carlson K; Veile R; Mishra SK; Wells SA; Donis-Keller H
Proc Natl Acad Sci U S A; 1993 Jan; 90(2):492-6. PubMed ID: 8093642
[TBL] [Abstract][Full Text] [Related]
57. Relationship of the human protooncogene CBL2 on 11q23 to the t(4;11), t(11;22), and t(11;14) breakpoints.
Savage PD; Shapiro M; Langdon WY; Geurts van Kessel AD; Seuanez HN; Akao Y; Croce C; Morse HC; Kersey JH
Cytogenet Cell Genet; 1991; 56(2):112-5. PubMed ID: 2013228
[TBL] [Abstract][Full Text] [Related]
58. A radiation hybrid map of 95 STSs spanning human chromosome 13q.
Shaw SH; Farr JE; Thiel BA; Matise TC; Weissenbach J; Chakaravarti A; Richard CW
Genomics; 1995 Jun; 27(3):502-10. PubMed ID: 7558033
[TBL] [Abstract][Full Text] [Related]
59. Alpha-chain locus of the T-cell antigen receptor is involved in the t(10;14) chromosome translocation of T-cell acute lymphocytic leukemia.
Kagan J; Finan J; Letofsky J; Besa EC; Nowell PC; Croce CM
Proc Natl Acad Sci U S A; 1987 Jul; 84(13):4543-6. PubMed ID: 2885838
[TBL] [Abstract][Full Text] [Related]
60. Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24.
Flejter WL; Watkins M; Abel KJ; Chandrasekharappa SC; Weber BL; Collins FS; Glover TW
Cytogenet Cell Genet; 1993; 64(3-4):222-3. PubMed ID: 8404043
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
