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 *

157 related articles for article (PubMed ID: 15801390)

  • 1. [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]  

  • 2. [Fragile X syndrome. Diagnosis, genetics and clinical findings].
    Hjalgrim H; Grønskov K; Brøndum-Nielsen K
    Ugeskr Laeger; 1998 Sep; 160(37):5330-4. PubMed ID: 9748856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Maximizing the sensitivity of a screening questionnaire for determining Fragile X at-risk status.
    Teisl JT; Reiss AL; Mazzocco MM
    Am J Med Genet; 1999 Apr; 83(4):281-5. PubMed ID: 10208162
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile X and company: finding the right diagnosis.
    Subramony SH; Friedrich CA; Jankowiak J
    Neurology; 2005 Jul; 65(2):E3-4. PubMed ID: 16043779
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. [Early diagnosis of fragile X mental retardation syndrome].
    Kan CC; Maaswinkel-Mooij PD; Veenema H
    Tijdschr Kindergeneeskd; 1990 Oct; 58(5):159-64. PubMed ID: 2247878
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Screening for fragile X syndrome among Brazilian mentally retarded male patients using PCR from buccal cell DNA.
    Christofolini DM; Lipay MV; Ramos MA; Brunoni D; Melaragno MI
    Genet Mol Res; 2006 Jul; 5(3):448-53. PubMed ID: 17117359
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Effectiveness of a clinical test in the preselection of children with suspected fragile X syndrome].
    Fernández Carvajal I; Blanco Quirós A; Fernández Toral J; Tellería Orriols JJ; Alonso Ramos MJ; Sanz Cantalapiedra A; Martín Rodríguez JF; Palencia Luances R
    An Esp Pediatr; 2001 Apr; 54(4):326-30. PubMed ID: 11273815
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Aspects of cognition and language in children with fragile X syndrome].
    Ferrando-Lucas MT; Banús-Gómez P; López-Pérez G
    Rev Neurol; 2003 Feb; 36 Suppl 1():S137-42. PubMed ID: 12599115
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Contribution of social and information-processing factors to eye-gaze avoidance in fragile X syndrome.
    Murphy MM; Abbeduto L; Schroeder S; Serlin R
    Am J Ment Retard; 2007 Sep; 112(5):349-60. PubMed ID: 17676959
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Screening for the fragile X syndrome: the necessity of international guidelines for molecular genetics predictive testing in general.
    Fryns JP
    Genet Couns; 1995; 6(4):293-6. PubMed ID: 8775414
    [No Abstract]   [Full Text] [Related]  

  • 13. [A clinical and molecular genetic analysis of the fragile X syndrome].
    Bychkova AM; Maliarchuk SG; Livshits LA
    Tsitol Genet; 1999; 33(4):70-6. PubMed ID: 10563381
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fragile X syndrome: recognition in young children.
    Simko A; Hornstein L; Soukup S; Bagamery N
    Pediatrics; 1989 Apr; 83(4):547-52. PubMed ID: 2927995
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis and management of fragile X syndrome.
    Wattendorf DJ; Muenke M
    Am Fam Physician; 2005 Jul; 72(1):111-3. PubMed ID: 16035691
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [The fragile chromosome X syndrome].
    Seemanová E; Passarge E; Schmidt A; Hyánek J; Salichová J
    Cas Lek Cesk; 1982 Oct; 121(40):1238-41. PubMed ID: 7139686
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Variable expression of clinical features of Martin Bell syndrome in younger patients.
    Verma IC; Elango R
    Indian Pediatr; 1994 Apr; 31(4):433-8. PubMed ID: 7875865
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.