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.
238 related articles for article (PubMed ID: 2612208)
1. A somatic cell hybrid mapping panel for regional assignment of human chromosome 13 DNA sequences. Cowell JK; Mitchell CD Cytogenet Cell Genet; 1989; 52(1-2):1-6. PubMed ID: 2612208 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. A somatic cell hybrid map of human chromosome 13. Washington SS; Bowcock AM; Gerken S; Matsunami N; Lesh D; Osborne-Lawrence SL; Cowell J; Ledbetter DH; White RL; Chakravarti A Genomics; 1993 Dec; 18(3):486-95. PubMed ID: 8307557 [TBL] [Abstract][Full Text] [Related]
4. Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14. Mitchell CD; Cowell JK Hum Genet; 1988 Dec; 81(1):57-60. PubMed ID: 3198126 [TBL] [Abstract][Full Text] [Related]
5. Carboxyl ester lipase: a highly polymorphic locus on human chromosome 9qter. Taylor AK; Zambaux JL; Klisak I; Mohandas T; Sparkes RS; Schotz MC; Lusis AJ Genomics; 1991 Jun; 10(2):425-31. PubMed ID: 1676983 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. A chromosomal breakpoint that separates the esterase D and retinoblastoma predisposition loci in a patient with del(13)(q14q31). Cowell JK; Hungerford J; Rutland P; Jay M Cancer Genet Cytogenet; 1987 Jul; 27(1):27-31. PubMed ID: 3472646 [TBL] [Abstract][Full Text] [Related]
8. Localization of ESD and A2M genes to sheep chromosome 3 by in situ hybridization. Graphodatsky AS; Biltueva LS; Filippov VA; Eremina VR; Lushnikova TP; Shumny TV; Ermolaev VI Cytogenet Cell Genet; 1993; 62(2-3):156-8. PubMed ID: 7679066 [TBL] [Abstract][Full Text] [Related]
9. Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridization. Duncan AM; Morgan C; Gallie Bl; Phillips RA; Squire J Cytogenet Cell Genet; 1987; 44(2-3):153-7. PubMed ID: 3032521 [TBL] [Abstract][Full Text] [Related]
10. Late replication studies and esterase D levels in a case of unbalanced X;autosome translocation, 46,X,t(X;13)(q27;q12). Romain DR; Columbano-Green LM; Parfitt RG; Smythe RH; MacKenzie NG; Chapman CJ J Med Genet; 1988 Oct; 25(10):716-8. PubMed ID: 3225828 [No Abstract] [Full Text] [Related]
11. Integration site(s) of herpes simplex virus type 1 thymidine kinase gene and regional assignment of the gene for aminoacylase-1 in human chromosomes. Kit S; Hazen M; Qavi H; Dubbs DR; Pathak S Cytogenet Cell Genet; 1980; 26(2-4):93-103. PubMed ID: 6248297 [TBL] [Abstract][Full Text] [Related]
12. Development and utilization of a somatic cell hybrid mapping panel to assign NotI linking probes to the long arm of human chromosome 6. Meese EU; Witkowski CM; Zoghbi HY; Stanbridge EJ; Meltzer PS; Trent JM Genomics; 1992 Mar; 12(3):542-8. PubMed ID: 1559705 [TBL] [Abstract][Full Text] [Related]
13. Assignment of rat linkage group V to chromosome 19 by single-strand conformation polymorphism analysis of somatic cell hybrids. Pravenec M; Simonet L; Kren V; St Lezin E; Levan G; Szpirer J; Szpirer C; Kurtz T Genomics; 1992 Feb; 12(2):350-6. PubMed ID: 1740344 [TBL] [Abstract][Full Text] [Related]
14. Assignment of the human gene for CREB1 to chromosome 2q32.3-q34. Taylor AK; Klisak I; Mohandas T; Sparkes RS; Li C; Gaynor R; Lusis AJ Genomics; 1990 Jul; 7(3):416-21. PubMed ID: 2142119 [TBL] [Abstract][Full Text] [Related]
15. An expanded mouse-human hybrid cell panel for mapping human chromosome 16. Callen DF; Baker E; Eyre HJ; Lane SA Ann Genet; 1990; 33(4):190-5. PubMed ID: 2095701 [TBL] [Abstract][Full Text] [Related]
16. A hybrid cell mapping panel for regional localization of probes to human chromosome 8. Wagner MJ; Ge Y; Siciliano M; Wells DE Genomics; 1991 May; 10(1):114-25. PubMed ID: 2045096 [TBL] [Abstract][Full Text] [Related]
17. Assignment of human aldolase C gene to chromosome 17, region cen----q21.1. Rocchi M; Vitale E; Covone A; Romeo G; Santamaria R; Buono P; Paolella G; Salvatore F Hum Genet; 1989 Jun; 82(3):279-82. PubMed ID: 2731939 [TBL] [Abstract][Full Text] [Related]
18. Isolation of chromosome-specific DNA sequences from an Alu polymerase chain reaction library to define the breakpoint in a patient with a constitutional translocation t(1;13) (q22;q12) and ganglioneuroblastoma. Michalski AJ; Cotter FE; Cowell JK Oncogene; 1992 Aug; 7(8):1595-602. PubMed ID: 1630820 [TBL] [Abstract][Full Text] [Related]
19. Assignment of the human CD9 gene to chromosome 12 (region P13) by use of human specific DNA probes. Benoit P; Gross MS; Frachet P; Frézal J; Uzan G; Boucheix C; Nguyen VC Hum Genet; 1991 Jan; 86(3):268-72. PubMed ID: 1997380 [No Abstract] [Full Text] [Related]
20. Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STS. Roberts T; Mead RS; Cowell JK Ann Hum Genet; 1996 May; 60(3):213-20. PubMed ID: 8800437 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]