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 *

110 related articles for article (PubMed ID: 1458226)

  • 41. 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]  

  • 42. Transgenic mouse model for the fragile X syndrome.
    Kooy RF; D'Hooge R; Reyniers E; Bakker CE; Nagels G; De Boulle K; Storm K; Clincke G; De Deyn PP; Oostra BA; Willems PJ
    Am J Med Genet; 1996 Aug; 64(2):241-5. PubMed ID: 8844056
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Fragile X syndrome.
    Chakrabarti L; Davies KE
    Curr Opin Neurol; 1997 Apr; 10(2):142-7. PubMed ID: 9146995
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Fragile X syndrome is less common than previously estimated.
    Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; Bullock S
    J Med Genet; 1997 Jan; 34(1):1-5. PubMed ID: 9032640
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Segregation of the fragile X mutation from an affected male to his normal daughter.
    Willems PJ; Van Roy B; De Boulle K; Vits L; Reyniers E; Beck O; Dumon JE; Verkerk A; Oostra B
    Hum Mol Genet; 1992 Oct; 1(7):511-5. PubMed ID: 1307252
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Fragile X syndrome and fragile XE mental retardation.
    Sutherland GR; Mulley JC
    Prenat Diagn; 1996 Dec; 16(13):1199-211. PubMed ID: 9061751
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods.
    Tuckerman E; Webb T
    Clin Genet; 1989 Jul; 36(1):25-30. PubMed ID: 2766560
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Physical characteristics of young boys with fragile X syndrome: reasons for difficulties in making a diagnosis in young males.
    Lachiewicz AM; Dawson DV; Spiridigliozzi GA
    Am J Med Genet; 2000 Jun; 92(4):229-36. PubMed ID: 10842286
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
    Sutherland GR; Baker E
    Clin Genet; 1990 Mar; 37(3):167-72. PubMed ID: 2323087
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Carriers of fragile X syndrome can present with a broad spectrum of clinical disorders].
    Jønch AE; Grønskov K; Carlsen Lunding JM; Nielsen JE; Brøndum-Nielsen K
    Ugeskr Laeger; 2014 Jun; 176(26):V02140099. PubMed ID: 25294575
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Autism and the fragile X syndrome.
    Fisch GS; Cohen IL; Wolf EG; Brown WT; Jenkins EC; Gross A
    Am J Psychiatry; 1986 Jan; 143(1):71-3. PubMed ID: 3455802
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Pathology of unstable sequence of genome: fragile-X-syndrome].
    Beldjord C; Richard L
    C R Seances Soc Biol Fil; 1992; 186(4):363-70. PubMed ID: 1301224
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome.
    Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ
    Am J Ment Retard; 2004 May; 109(3):208-18. PubMed ID: 15072521
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Compound heterozygous female with fragile X syndrome.
    Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK
    Am J Med Genet; 1999 Apr; 83(4):318-21. PubMed ID: 10208169
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Fragile X chromosomes and fragile X syndrome].
    Boonen SE; Grønskov K; Brøndum-Nielsen K
    Ugeskr Laeger; 2006 Oct; 168(43):3727-8. PubMed ID: 17069739
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The X-inactivation imprinting model of the fragile-X syndrome: annotated references, 1990.
    Laird CD
    Prog Clin Biol Res; 1991; 368():101-10. PubMed ID: 1946501
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.
    Ryynänen M; Kirkinen P; Mannermaa A; Saarikoski S
    Am J Obstet Gynecol; 1995 Apr; 172(4 Pt 1):1236-9. PubMed ID: 7726262
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India.
    Jain U; Verma IC; Kapoor AK
    Indian J Med Res; 1998 Jul; 108():12-6. PubMed ID: 9745213
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Fragile X syndrome: molecular analysis reveals a new mechanism of mutation in human genetic diseases.
    Poustka A
    Ann Med; 1992 Dec; 24(6):453-6. PubMed ID: 1485937
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Memory skills of boys with fragile X syndrome.
    Ornstein PA; Schaaf JM; Hooper SR; Hatton DD; Mirrett P; Bailey DB
    Am J Ment Retard; 2008 Nov; 113(6):453-65. PubMed ID: 19127656
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.