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 *

186 related articles for article (PubMed ID: 26961978)

  • 1. Family Communication and Cascade Testing for Fragile X Syndrome.
    Raspa M; Edwards A; Wheeler AC; Bishop E; Bailey DB
    J Genet Couns; 2016 Oct; 25(5):1075-84. PubMed ID: 26961978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular screening for fragile X syndrome in Thailand.
    Limprasert P; Ruangdaraganon N; Sura T; Vasiknanonte P; Jinorose U
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():114-8. PubMed ID: 11400746
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey.
    Bailey DB; Raspa M; Bishop E; Holiday D
    Pediatrics; 2009 Aug; 124(2):527-33. PubMed ID: 19581269
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome.
    Sherman SL; Kidd SA; Riley C; Berry-Kravis E; Andrews HF; Miller RM; Lincoln S; Swanson M; Kaufmann WE; Brown WT
    Pediatrics; 2017 Jun; 139(Suppl 3):S183-S193. PubMed ID: 28814539
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Anxiety, attention problems, hyperactivity, and the Aberrant Behavior Checklist in fragile X syndrome.
    Wheeler A; Raspa M; Bann C; Bishop E; Hessl D; Sacco P; Bailey DB
    Am J Med Genet A; 2014 Jan; 164A(1):141-55. PubMed ID: 24352914
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detailed assessment of incontinence in boys with fragile-X-syndrome in a home setting.
    Niemczyk J; von Gontard A; Equit M; Bauer K; Naumann T; Wagner C; Curfs L
    Eur J Pediatr; 2016 Oct; 175(10):1325-34. PubMed ID: 27567619
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Discovering fragile X syndrome: family experiences and perceptions.
    Bailey DB; Skinner D; Sparkman KL
    Pediatrics; 2003 Feb; 111(2):407-16. PubMed ID: 12563071
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Informing members of families affected by fragile X syndrome of this diagnosis].
    Carrasco M
    Rev Neurol; 2001 Oct; 33 Suppl 1():S37-41. PubMed ID: 12447818
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Parent perspectives following newborn screening resulting in diagnoses of fragile X syndrome or fragile X premutation.
    Corbo A; Tzeng JP; Scott S; Cheves E; Cope H; Peay H
    Res Dev Disabil; 2024 May; 148():104719. PubMed ID: 38507982
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence, nature, and correlates of sleep problems among children with fragile X syndrome based on a large scale parent survey.
    Kronk R; Bishop EE; Raspa M; Bickel JO; Mandel DA; Bailey DB
    Sleep; 2010 May; 33(5):679-87. PubMed ID: 20469810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Psychopathology and familial stress - comparison of boys with Fragile X syndrome and spinal muscular atrophy.
    von Gontard A; Backes M; Laufersweiler-Plass C; Wendland C; Lehmkuhl G; Zerres K; Rudnik-Schöneborn S
    J Child Psychol Psychiatry; 2002 Oct; 43(7):949-57. PubMed ID: 12405482
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization, treatment patterns, and patient-related outcomes of patients with Fragile X syndrome in Germany: final results of the observational EXPLAIN-FXS study.
    Haessler F; Gaese F; Huss M; Kretschmar C; Brinkman M; Peters H; Elstner S; Colla M; Pittrow D
    BMC Psychiatry; 2016 Sep; 16(1):318. PubMed ID: 27612457
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hair root fragile X mental retardation protein assay for the diagnosis of fragile X syndrome].
    Luo XF; Zhong JM; Zhang XZ; Zou Y; Chen Y; Wu HP; Yu XY
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Oct; 11(10):817-20. PubMed ID: 19849940
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Elimination disorders in persons with Prader-Willi and Fragile-X syndromes.
    Equit M; Piro-Hussong A; Niemczyk J; Curfs L; von Gontard A
    Neurourol Urodyn; 2013 Sep; 32(7):986-92. PubMed ID: 23239431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of fragile X syndrome: a qualitative study of African American families.
    Visootsak J; Charen K; Rohr J; Allen E; Sherman S
    J Genet Couns; 2012 Dec; 21(6):845-53. PubMed ID: 22134579
    [TBL] [Abstract][Full Text] [Related]  

  • 16. When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.
    Wehbe RM; Spiridigliozzi GA; Heise EM; Dawson DV; McConkie-Rosell A
    Am J Med Genet A; 2009 Jun; 149A(6):1190-9. PubMed ID: 19449413
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Implications of the
    Wheeler A; Raspa M; Hagerman R; Mailick M; Riley C
    Pediatrics; 2017 Jun; 139(Suppl 3):S172-S182. PubMed ID: 28814538
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delayed diagnosis of fragile X syndrome--United States, 1990-1999.
    Centers for Disease Control and Prevention (CDC)
    MMWR Morb Mortal Wkly Rep; 2002 Aug; 51(33):740-2. PubMed ID: 12201607
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal attitudes to newborn screening for fragile X syndrome.
    Christie L; Wotton T; Bennetts B; Wiley V; Wilcken B; Rogers C; Boyle J; Turner C; Hansen J; Hunter M; Goel H; Field M
    Am J Med Genet A; 2013 Feb; 161A(2):301-11. PubMed ID: 23303663
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Women's attitudes toward testing for fragile X carrier status: a qualitative analysis.
    Anido A; Carlson LM; Taft L; Sherman SL
    J Genet Couns; 2005 Aug; 14(4):295-306. PubMed ID: 16047092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.