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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 8484403)

  • 21. Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23.
    Sutherland GR; Jacky PB; Baker E; Manuel A
    Am J Hum Genet; 1983 May; 35(3):432-7. PubMed ID: 6859039
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece.
    Mavrou A; Syrrou M; Tsenghi C; Metaxotou C
    Am J Med Genet; 1991; 38(2-3):437-9. PubMed ID: 2018086
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chromosomal fragile site expression in dogs: II. Expression in boxer dogs with mast cell tumors.
    Stone DM; Jacky PB; Prieur DJ
    Am J Med Genet; 1991 Aug; 40(2):223-9. PubMed ID: 1910264
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fragile site (16) (q22). III. Segregation analysis.
    Müller B; Feichtinger W; Bonaïti-Pellié C; Schmid M
    Hum Genet; 1992 Aug; 89(6):612-4. PubMed ID: 1511978
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A clinical and cytogenetic study of institutionalized mental retardates.
    Kumada T
    Hiroshima J Med Sci; 1990 Jun; 39(2):39-56. PubMed ID: 2228726
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Bromodeoxyuridine induces chromosomal fragile sites in the canine genome.
    Stone DM; Stephens KE
    Am J Med Genet; 1993 Apr; 46(2):198-202. PubMed ID: 8484410
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Marker X syndrome in an oriental family with probable transmission by a normal male.
    Rhoads FA; Oglesby AC; Mayer M; Jacobs PA
    Am J Med Genet; 1982 Jun; 12(2):205-17. PubMed ID: 7102725
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fragile sites on chromosomes.
    Hecht F; Glover TW; Kaiser-Hecht B
    Pediatrics; 1982 Jan; 69(1):121-3. PubMed ID: 6976555
    [No Abstract]   [Full Text] [Related]  

  • 29. The fragile X chromosome: current methods.
    Hecht F; Jacky PB; Sutherland GR
    Am J Med Genet; 1982 Apr; 11(4):489-95. PubMed ID: 6211983
    [No Abstract]   [Full Text] [Related]  

  • 30. Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites.
    Kähkönen M; Tengström C; Alitalo T; Matilainen R; Kaski M; Airaksinen E
    Hum Genet; 1989 Apr; 82(1):3-8. PubMed ID: 2714776
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A fragile site at 10q23 (FRA10A) in a phenytoin-exposed fetus: a case report and review of the literature.
    Morel CF; Duncan AM; Désilets V
    Prenat Diagn; 2005 Apr; 25(4):318-21. PubMed ID: 15849796
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Mental retardation and fragile site Xq27-28: 2 affected brothers and their mother within the framework of chromosome instability].
    Tarantino E; Spagesi D; Simi P; Fiori B
    Pathologica; 1983; 75 Suppl():331-4. PubMed ID: 6680436
    [No Abstract]   [Full Text] [Related]  

  • 33. Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22.
    Stoll C; Roy-Doray B; Dott B; Alembik Y
    Genet Couns; 1997; 8(2):115-20. PubMed ID: 9219009
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A new heritable fragile site at 15q13 in a three-generation family.
    Zamani AG; Durakbasi-Dursun HG; Acar A
    Cytogenet Genome Res; 2007; 116(4):252-5. PubMed ID: 17431322
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A folate sensitive heritable fragile site at 19p13.
    Tommerup N; Nielsen J; Mikkelsen M
    Clin Genet; 1985 May; 27(5):510-4. PubMed ID: 3159519
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Folate metabolism in cells from fragile X syndrome patients and carriers.
    Wang JC; Erbe RW
    Am J Med Genet; 1984 Jan; 17(1):303-10. PubMed ID: 6585141
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The role of nucleotides in human fragile site expression.
    Sutherland GR
    Mutat Res; 1988; 200(1-2):207-13. PubMed ID: 3292907
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Inability to induce fragile sites at CTG repeats in congenital myotonic dystrophy.
    Wenger SL; Giangreco CA; Tarleton J; Wessel HB
    Am J Med Genet; 1996 Dec; 66(1):60-3. PubMed ID: 8957513
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes.
    Smeets DF; Merkx G
    Hum Genet; 1990 Nov; 86(1):76-8. PubMed ID: 2253942
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fra(2) (q13) and inv(9) (p11q12) in autism: causal relationship?
    Jayakar P; Chudley AE; Ray M; Evans JA; Perlov J; Wand R
    Am J Med Genet; 1986; 23(1-2):381-92. PubMed ID: 3953656
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.