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2. [Fragile sites on human chromosomes and cancer-specific chromosomal rearrangements]. Hori T. Gan To Kagaku Ryoho; 1986 Mar; 13(3 Pt 2):667-76. PubMed ID: 3963838 [Abstract] [Full Text] [Related]
3. Implications of fragile X expression in normal males for the nature of the mutation. Ledbetter DH, Ledbetter SA, Nussbaum RL. Nature; 1986 Mar; 324(6093):161-3. PubMed ID: 3785381 [Abstract] [Full Text] [Related]
5. Fragile X expression in thymidine-prototrophic and auxotrophic human-mouse somatic cell hybrids under low and high thymidylate stress conditions. Hori T, Takahashi E, Tsuji H, Tsuji S, Murata M. Cytogenet Cell Genet; 1988 Mar; 47(4):177-80. PubMed ID: 3416651 [Abstract] [Full Text] [Related]
7. Assignment of human gene encoding thymidylate synthase to chromosome 18 using interspecific cell hybrids between thymidylate synthase-negative mouse mutant cells and human diploid fibroblasts. Hori T, Ayusawa D, Shimizu K, Koyama H, Seno T. Somat Cell Mol Genet; 1985 May; 11(3):277-83. PubMed ID: 3859022 [Abstract] [Full Text] [Related]
8. Expression of fragile X chromosome in human-rodent somatic cell hybrids. Warren ST, Davidson RL. Somat Cell Mol Genet; 1984 Jul; 10(4):409-13. PubMed ID: 6589793 [Abstract] [Full Text] [Related]
9. Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X). Daniel A, Ekblom L, Phillips S. Am J Med Genet; 1984 Jul; 18(3):483-91. PubMed ID: 6476008 [Abstract] [Full Text] [Related]
10. Antifolate-induced misincorporation of deoxyuridine monophosphate into DNA by cells from patients with the fragile X syndrome. Wang JC, Beardsley GP, Erbe RW. Am J Med Genet; 1985 Aug; 21(4):691-6. PubMed ID: 2992271 [Abstract] [Full Text] [Related]
11. Excess thymidine induces folate sensitive fragile sites. Sutherland GR, Baker E, Fratini A. Am J Med Genet; 1985 Oct; 22(2):433-43. PubMed ID: 4050872 [Abstract] [Full Text] [Related]
12. [Variations in the presence of a fragile site on X--fra(X)--according to cases and methods used]. Crippa L, Delozier-Blanchet CD, Engel E. J Genet Hum; 1984 Jul; 32(3):193-7. PubMed ID: 6481341 [Abstract] [Full Text] [Related]
13. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males. Soudek D, Partington MW, Lawson JS. Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598 [Abstract] [Full Text] [Related]
14. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome. Ventruto V, Stabile M, Gentile G, de Tollis G, Colantuoni M, Sirone P, Perone L, Lonardo F, Della Monica M, Fiore M. Ann Genet; 1986 Jan; 29(1):59-61. PubMed ID: 3487280 [Abstract] [Full Text] [Related]
15. 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]
16. Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid. Nussbaum RL, Airhart SD, Ledbetter DH. Hum Genet; 1983 May; 64(2):148-50. PubMed ID: 6885049 [Abstract] [Full Text] [Related]
17. Chromosome breakage induced by thymidylate stress in thymidylate synthase-negative mutants of mouse FM3A cells. Hori T, Ayusawa D, Shimizu K, Koyama H, Seno T. Cancer Res; 1984 Feb; 44(2):703-9. PubMed ID: 6692373 [Abstract] [Full Text] [Related]
18. Caffeine enhances fragile (X) expression in somatic cell hybrids. Ledbetter DH, Airhart SD, Nussbaum RL. Am J Med Genet; 1986 Feb; 23(1-2):445-55. PubMed ID: 2937299 [Abstract] [Full Text] [Related]
19. Expression of fragile X in human-mouse somatic cell hybrids. Lin MS, Shimanuki K, Wilson MG. Cytogenet Cell Genet; 1987 Feb; 44(2-3):118-22. PubMed ID: 3568760 [Abstract] [Full Text] [Related]
20. Triradial configurations indicate that expression of the fragile site at Xq27 is non-lethal. Tommerup N. Ann Genet; 1987 Feb; 30(4):231-2. PubMed ID: 3501266 [Abstract] [Full Text] [Related] Page: [Next] [New Search]