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 *

123 related articles for article (PubMed ID: 3177457)

  • 21. Recent experience in prenatal diagnosis of fragile X.
    Howard-Peebles PN; Maddalena A
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):162-6. PubMed ID: 1605186
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fragile X-linked mental retardation of macro-orchidism.
    Moore BC; Glover TW; Kaiser-McCaw B; Hecht F
    West J Med; 1982 Oct; 137(4):278-81. PubMed ID: 7179944
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studies.
    Murphy PD; Wilmot PL; Shapiro LR
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):181-6. PubMed ID: 1605190
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Induction of the fra(X) in amniotic fluid cells by excess thymidine.
    Tommerup N
    Am J Med Genet; 1988; 30(1-2):451-3. PubMed ID: 3052068
    [No Abstract]   [Full Text] [Related]  

  • 25. Prenatal diagnosis and carrier screening for fragile X by PCR.
    Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Stark-Houck S; Brophy P; Duncan C; Dobkin C; Jenkins E
    Am J Med Genet; 1996 Jul; 64(1):191-5. PubMed ID: 8826474
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].
    Benítez J; Fernández E; Ramos C; Nunes V; del Río E; Baiget M
    Rev Clin Esp; 1989 Apr; 184(7):364-6. PubMed ID: 2570446
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fra(X) prenatal diagnosis: are endoreduplicated and polyploid cells useful diagnostic criteria?
    Krawczun MS; Duncan CJ; Stark-Houck SL; Jenkins EC
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):149-54. PubMed ID: 1605184
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of fragile (X) syndrome.
    Hogge WA; Schonberg SA; Glover TW; Hecht F; Golbus MS
    Obstet Gynecol; 1984 Mar; 63(3 Suppl):19S-21S. PubMed ID: 6700875
    [TBL] [Abstract][Full Text] [Related]  

  • 30. First trimester prenatal diagnosis of a male fetus with fragile X.
    Tommerup N; Søndergaard F; Tønnesen T; Kristensen M; Arveiler B; Schinzel A
    Lancet; 1985 Apr; 1(8433):870. PubMed ID: 2858725
    [No Abstract]   [Full Text] [Related]  

  • 31. Prenatal cytogenetic diagnosis of the fragile X chromosome: feasibility and speed of in situ clonal method in amniotic fluid cell tissue culture.
    Shapiro LR; Wilmot PL; Andree LE
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):167-9. PubMed ID: 1605187
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.
    Webb T; Gosden CM; Rodeck CH; Hamill MA; Eason PE
    Prenat Diagn; 1983; 3(2):131-7. PubMed ID: 6622392
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes.
    Rocchi M; Pecile V; Archidiacono N; Monni G; Dumez Y; Filippi G
    Prenat Diagn; 1985; 5(3):229-31. PubMed ID: 4022944
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis of the fragile X syndrome using fetal blood and amniotic fluid.
    Webb TP; Rodeck CH; Nicolaides KH; Gosden CM
    Prenat Diagn; 1987 Mar; 7(3):203-14. PubMed ID: 3588539
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The strength of association between fragile (X) chromosome presence and mental retardation.
    Silverman W; Lubin R; Jenkins EC; Brown WT
    Clin Genet; 1983 Jun; 23(6):436-40. PubMed ID: 6684008
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal detection of fra(X)(q27.3) in female identical twins: reliability of low level cytogenetic prenatal expression in females.
    Jenkins EC; Brown WT; Schonberg S; Krawczun MS; Goldberg J; Golbus MS
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):128-35. PubMed ID: 1605181
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
    Jenkins EC; Genovese MJ; Duncan CJ; Gu H; Stark-Houck SL; Lele K; Li SY; Krawczun MS
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):136-41. PubMed ID: 1605182
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fragile X expression in normal and mentally retarded subjects: effect of treatment with an antifolic agent.
    Sanfilippo S; Ragusa RM; Scillato F; Ruggeri M; Neri G
    Am J Med Genet; 1988; 30(1-2):369-76. PubMed ID: 3177459
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fragile X syndrome: a public health concern.
    Trusler S; Beatty-DeSana J
    Am J Public Health; 1985 Jul; 75(7):771-2. PubMed ID: 4003653
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.
    Oberlé I; Mandel JL; Boué J; Mattei MG; Mattei JF
    Lancet; 1985 Apr; 1(8433):871. PubMed ID: 2858726
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.