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Journal Abstract Search
121 related items for PubMed ID: 2543620
1. Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci. Keyeux G, Gilgenkrantz S, Lefranc G, Lefranc MP. Hum Genet; 1989 Jun; 82(3):219-22. PubMed ID: 2543620 [Abstract] [Full Text] [Related]
2. Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplication. Keyeux G, Gilgenkrantz S, Lefranc G, Lefranc MP. Hum Genet; 1990 Oct; 85(6):617-22. PubMed ID: 1977685 [Abstract] [Full Text] [Related]
3. Physical mapping of probes within 14q32, a subtelomeric region showing a high recombination frequency. Hofker MH, Smith S, Nakamura Y, Teshima I, White R, Cox DW. Genomics; 1990 Jan; 6(1):33-8. PubMed ID: 2303262 [Abstract] [Full Text] [Related]
4. Molecular characterization of ataxia telangiectasia T cell clones. III. Mapping the 14q32.1 distal breakpoint. Stern MH, Zhang FR, Thomas G, Griscelli C, Aurias A. Hum Genet; 1988 Dec; 81(1):18-22. PubMed ID: 3264259 [Abstract] [Full Text] [Related]
5. Analysis of a break in chromosome 14 mapping to the region of the immunoglobulin heavy chain locus. Linsley PS, Bech-Hansen NT, Siminovitch L, Cox DW. Proc Natl Acad Sci U S A; 1983 Apr; 80(7):1997-2001. PubMed ID: 6403943 [Abstract] [Full Text] [Related]
6. Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Purrello M, Alhadeff B, Whittington E, Buckton KE, Daniel A, Arnaud P, Rocchi M, Archidiacono N, Filippi G, Siniscalco M. Cytogenet Cell Genet; 1987 Apr; 44(1):32-40. PubMed ID: 3469062 [Abstract] [Full Text] [Related]
11. Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of Pi(alpha 1-antitrypsin). Yamamoto Y, Sawa R, Okamoto N, Matsui A, Yanagisawa M, Ikemoto S. Hum Genet; 1986 Oct; 74(2):190-2. PubMed ID: 3490426 [Abstract] [Full Text] [Related]
12. Identification of novel cryptic translocations involving IGH in B-cell non-Hodgkin's lymphomas. Gozzetti A, Davis EM, Espinosa R, Fernald AA, Anastasi J, Le Beau MM. Cancer Res; 2002 Oct 01; 62(19):5523-7. PubMed ID: 12359763 [Abstract] [Full Text] [Related]
13. Physical mapping of four serpin genes: alpha 1-antitrypsin, alpha 1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome I4q32.1. Billingsley GD, Walter MA, Hammond GL, Cox DW. Am J Hum Genet; 1993 Feb 01; 52(2):343-53. PubMed ID: 8381582 [Abstract] [Full Text] [Related]
15. Recurrent breakpoints in 14q32.13/TCL1A region in mature B-cell neoplasms with villous lymphocytes. Urbankova H, Baens M, Michaux L, Tousseyn T, Rack K, Katrincsakova B, Ferreiro JF, van Loo P, de Kelver W, Dierickx D, Demuynck H, Delannoy A, Verschuere J, Jarošová M, de Wolf-Peeters C, Vandenberghe P, Wlodarska I. Leuk Lymphoma; 2012 Dec 01; 53(12):2449-55. PubMed ID: 22553924 [Abstract] [Full Text] [Related]
17. Physical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiency. Byth BC, Billingsley GD, Cox DW. Am J Hum Genet; 1994 Jul 01; 55(1):126-33. PubMed ID: 7912884 [Abstract] [Full Text] [Related]