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 *

118 related articles for article (PubMed ID: 15915189)

  • 1. Prenatal genetic testing: full clinical information is needed.
    Harraway J
    N Z Med J; 2005 May; 118(1215):U1468. PubMed ID: 15915189
    [No Abstract]   [Full Text] [Related]  

  • 2. [Gene diagnosis of fragile X syndrome].
    Wu G; Shen Y
    Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):698-700. PubMed ID: 9639773
    [No Abstract]   [Full Text] [Related]  

  • 3. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection.
    Dobkin C; Ding X; Li S; Houck G; Nolin SL; Glicksman A; Zhong N; Jenkins EC; Brown WT
    Am J Med Genet; 1999 Apr; 83(4):338-41. PubMed ID: 10208176
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
    Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
    Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.
    Berkenstadt M; Ries-Levavi L; Cuckle H; Peleg L; Barkai G
    Prenat Diagn; 2007 Nov; 27(11):991-4. PubMed ID: 17705235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Three peaks in the polymerase chain reaction fragile X analysis.
    Sharony R; Shtorch A; Amiel A; Guetta E; Peleg L; Pras E; Ries-Levavi L
    J Med Screen; 2012 Sep; 19(3):112-5. PubMed ID: 23093728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Detection of fragile X syndrome by molecular hybridization in 29 families affected by hereditary mental retardation].
    Masmoudi S; Keskes L; Feki I; Fakhfakh F; Triki C; Ghribi F; Mhiri C; Ayadi H
    Tunis Med; 1998; 76(8-9):244-9. PubMed ID: 9810860
    [No Abstract]   [Full Text] [Related]  

  • 8. Population-based carrier screening and prenatal diagnosis.
    Strom CM
    MLO Med Lab Obs; 2004 Aug; 36(8):12-7; quiz 20-1. PubMed ID: 15366363
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal genetic counseling: what is fragile X?
    Bodurtha J; Tams L; Jackson-Cook C
    Va Med Q; 1992; 119(2):97-8. PubMed ID: 1562624
    [No Abstract]   [Full Text] [Related]  

  • 10. Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.
    Sutherland GR; Gedeon A; Kornman L; Donnelly A; Byard RW; Mulley JC; Kremer E; Lynch M; Pritchard M; Yu S
    N Engl J Med; 1991 Dec; 325(24):1720-2. PubMed ID: 1944473
    [No Abstract]   [Full Text] [Related]  

  • 11. [Fragile X syndrome: molecular aspects and prenatal diagnosis].
    Yeshaya-Shany J; Shalgi R; Mashiach S; Goldman B; Ravia Y
    Harefuah; 1995 May; 128(9):587-91. PubMed ID: 7797163
    [No Abstract]   [Full Text] [Related]  

  • 12. Fragile X syndrome: diagnostic and carrier testing. Working Group of the Genetic Screening Subcommittee of the Clinical Practice Committee. American College of Medical Genetics.
    Am J Med Genet; 1994 Dec; 53(4):380-1. PubMed ID: 7864050
    [No Abstract]   [Full Text] [Related]  

  • 13. Laboratory aspects of prenatal fra(X) detection.
    Jenkins EC; Krawczun MS; Brooks SE; Brooks SL; Sherman SL; Brown WT
    Prog Clin Biol Res; 1991; 368():27-42. PubMed ID: 1835094
    [No Abstract]   [Full Text] [Related]  

  • 14. [Problems posed by genetic diseases, concerning DNA instability disorders: fragile X syndrome].
    Lesca G; Rousselle C
    Rev Prat; 2006 Oct; 56(15):1705-10. PubMed ID: 17137259
    [No Abstract]   [Full Text] [Related]  

  • 15. [X fragile syndrome; how to make a precocious diagnostic].
    Gérard-Blanluet M
    Rev Prat; 2005 Jan; 55(1):7-12. PubMed ID: 15801390
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.
    Bastaki LA; Hegazy F; Al-Heneidi MM; Turki N; Azab AS; Naguib KK
    East Mediterr Health J; 2004; 10(1-2):116-24. PubMed ID: 16201716
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Screening for fragile X syndrome. International experiences].
    Vuust J; Larsen LA; Grønskov K; Nørgaard-Pedersen B; Brøndum-Nielsen K
    Ugeskr Laeger; 2006 Oct; 168(43):3704-9. PubMed ID: 17069733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular diagnosis of Fragile X syndrome.
    Sofocleous C; Kolialexi A; Mavrou A
    Expert Rev Mol Diagn; 2009 Jan; 9(1):23-30. PubMed ID: 19099346
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening for fragile X syndrome: information needs for health planners.
    Murray J; Cuckle H; Taylor G; Hewison J
    J Med Screen; 1997; 4(2):60-94. PubMed ID: 9275266
    [No Abstract]   [Full Text] [Related]  

  • 20. Who should be tested for fragile X carriership? A review of 1 center's pedigrees.
    Rajendra K; Bringman JJ; Ward J; Phillips OP
    Am J Obstet Gynecol; 2008 May; 198(5):e51-3. PubMed ID: 18358452
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.