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161 related items for PubMed ID: 2378345
1. Microdissection of the fragile X region. MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE. Am J Hum Genet; 1990 Aug; 47(2):181-6. PubMed ID: 2378345 [Abstract] [Full Text] [Related]
2. Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage. Warren ST, Knight SJ, Peters JF, Stayton CL, Consalez GG, Zhang FP. Proc Natl Acad Sci U S A; 1990 May; 87(10):3856-60. PubMed ID: 2339126 [Abstract] [Full Text] [Related]
3. Linear order of new and established DNA markers around the fragile site at Xq27.3. Hirst MC, Roche A, Flint TJ, MacKinnon RN, Bassett JH, Nakahori Y, Watson JE, Bell MV, Patterson MN, Boyd Y. Genomics; 1991 May; 10(1):243-9. PubMed ID: 2045104 [Abstract] [Full Text] [Related]
4. A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile site. Nussbaum RL, Airhart SD, Ledbetter DH. Am J Med Genet; 1986 May; 23(1-2):457-66. PubMed ID: 2937300 [Abstract] [Full Text] [Related]
5. Thymidylate synthase-deficient Chinese hamster cells: a selection system for human chromosome 18 and experimental system for the study of thymidylate synthase regulation and fragile X expression. Nussbaum RL, Walmsley RM, Lesko JG, Airhart SD, Ledbetter DH. Am J Hum Genet; 1985 Nov; 37(6):1192-205. PubMed ID: 3002173 [Abstract] [Full Text] [Related]
6. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Mulligan LM, Phillips MA, Forster-Gibson CJ, Beckett J, Partington MW, Simpson NE, Holden JJ, White BN. Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332 [Abstract] [Full Text] [Related]
7. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. Suthers GK, Hyland VJ, Callen DF, Oberle I, Rocchi M, Thomas NS, Morris CP, Schwartz CE, Schmidt M, Ropers HH. Am J Hum Genet; 1990 Aug; 47(2):187-95. PubMed ID: 2378346 [Abstract] [Full Text] [Related]
8. Physical map of human Xq27-qter: localizing the region of the fragile X mutation. Poustka A, Dietrich A, Langenstein G, Toniolo D, Warren ST, Lehrach H. Proc Natl Acad Sci U S A; 1991 Oct 01; 88(19):8302-6. PubMed ID: 1924290 [Abstract] [Full Text] [Related]
11. In situ hybridization studies using a molecular probe that maps to Xq27-Zq28. Duncan AM, Morgan C. Hum Genet; 1990 Apr 01; 84(5):446-8. PubMed ID: 2323777 [Abstract] [Full Text] [Related]
13. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site. Nguyen C, Mattei MG, Rey JA, Baeteman MA, Mattei JF, Jordan BR. Am J Med Genet; 1988 Apr 01; 30(1-2):601-11. PubMed ID: 2902799 [Abstract] [Full Text] [Related]
14. Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this region. Djabali M, Nguyen C, Biunno I, Oostra BA, Mattei MG, Ikeda JE, Jordan BR. Genomics; 1991 Aug 01; 10(4):1053-60. PubMed ID: 1916812 [Abstract] [Full Text] [Related]
15. New somatic cell hybrids for physical mapping in distal Xq and the fragile X region. Ledbetter SA, Schwartz CE, Davies KE, Ledbetter DH. Am J Med Genet; 1991 Aug 01; 38(2-3):418-20. PubMed ID: 2018083 [Abstract] [Full Text] [Related]
17. Strategy for molecular cloning of the fragile X site DNA. Warren ST, Zhang FP, Sutcliffe JS, Peters JF. Am J Med Genet; 1988 Aug 01; 30(1-2):613-23. PubMed ID: 3177473 [Abstract] [Full Text] [Related]
18. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3. Patterson M, Bell M, Schwartz C, Davies K. Am J Med Genet; 1988 Aug 01; 30(1-2):581-91. PubMed ID: 3177471 [Abstract] [Full Text] [Related]