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 *

153 related articles for article (PubMed ID: 8429429)

  • 1. Molecular genetic advances in fragile X syndrome.
    Tarleton JC; Saul RA
    J Pediatr; 1993 Feb; 122(2):169-85. PubMed ID: 8429429
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG; Hussein IR; Abuzenadah A; Gari M; Bassiouni R; Sogaty S; Lary S; Al-Quaiti M; Al Balwi M; Al Qahtani M
    Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular screening for fragile X syndrome in mentally handicapped children in Korea.
    Kwon SH; Lee KS; Hyun MC; Song KE; Kim JK
    J Korean Med Sci; 2001 Jun; 16(3):271-5. PubMed ID: 11410685
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The fragile X chromosome syndrome: DNA analysis in families with familial occurrence of mental retardation].
    Poláková H; Khoury L; Cierna M
    Bratisl Lek Listy; 1997 Mar; 98(3):150-6. PubMed ID: 9264820
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The fragile X syndrome.
    de Vries BB; Halley DJ; Oostra BA; Niermeijer MF
    J Med Genet; 1998 Jul; 35(7):579-89. PubMed ID: 9678703
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnostic, carrier and prenatal genetic testing for fragile X syndrome and other FMR-1-related disorders in Johannesburg, South Africa: a 20-year review.
    Essop FB; Krause A
    S Afr Med J; 2013 Oct; 103(12 Suppl 1):994-8. PubMed ID: 24300646
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The diagnosis of mental retardation in fragile X syndrome is revolutionized by molecular genetics].
    Lemire M; Rousseau F
    Union Med Can; 1993; 122(1):23-9. PubMed ID: 8465472
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [X-linked mental retardation: variations in the fragile X mutations and genetic counseling].
    Kondo I; Kurokawa Y
    Nihon Koshu Eisei Zasshi; 1993 Aug; 40(8):599-605. PubMed ID: 8219287
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Newborn, carrier, and early childhood screening recommendations for fragile X.
    Abrams L; Cronister A; Brown WT; Tassone F; Sherman SL; Finucane B; McConkie-Rosell A; Hagerman R; Kaufmann WE; Picker J; Coffey S; Skinner D; Johnson V; Miller R; Berry-Kravis E
    Pediatrics; 2012 Dec; 130(6):1126-35. PubMed ID: 23129072
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Fragile X syndrome (review).
    Pimentel MM
    Int J Mol Med; 1999 Jun; 3(6):639-45. PubMed ID: 10341296
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G; Mattei MG; Mattei JF; Jaye M; Mandel JL
    Nature; 1983 Dec 15-21; 306(5944):701-4. PubMed ID: 6689201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Advances in molecular analysis of fragile X syndrome.
    Warren ST; Nelson DL
    JAMA; 1994 Feb; 271(7):536-42. PubMed ID: 8301769
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
    Bell MV; Hirst MC; Nakahori Y; MacKinnon RN; Roche A; Flint TJ; Jacobs PA; Tommerup N; Tranebjaerg L; Froster-Iskenius U
    Cell; 1991 Feb; 64(4):861-6. PubMed ID: 1997211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening for fragile X syndrome.
    Murray J; Cuckle H; Taylor G; Hewison J
    Health Technol Assess; 1997; 1(4):i-iv, 1-71. PubMed ID: 9414543
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Disabilities caused by unstable mutations in Costa Rica.
    Cuenca P; Morales F; Castro I
    Rev Biol Trop; 2004 Sep; 52(3):501-5. PubMed ID: 17361543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.
    Rousseau F; Heitz D; Biancalana V; Blumenfeld S; Kretz C; Boué J; Tommerup N; Van Der Hagen C; DeLozier-Blanchet C; Croquette MF
    N Engl J Med; 1991 Dec; 325(24):1673-81. PubMed ID: 1944467
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.