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 *

398 related articles for article (PubMed ID: 28814537)

  • 1. Public Health Literature Review of Fragile X Syndrome.
    Raspa M; Wheeler AC; Riley C
    Pediatrics; 2017 Jun; 139(Suppl 3):S153-S171. PubMed ID: 28814537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Research Gaps in Fragile X Syndrome: An Updated Literature Review to Inform Clinical and Public Health Practice.
    Raspa M; Wheeler A; Okoniewski KC; Edwards A; Scott S
    J Dev Behav Pediatr; 2023 Jan; 44(1):e56-e65. PubMed ID: 36219479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Health supervision for children with fragile X syndrome.
    Hersh JH; Saul RA;
    Pediatrics; 2011 May; 127(5):994-1006. PubMed ID: 21518720
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A review of fragile X premutation disorders: expanding the psychiatric perspective.
    Bourgeois JA; Coffey SM; Rivera SM; Hessl D; Gane LW; Tassone F; Greco C; Finucane B; Nelson L; Berry-Kravis E; Grigsby J; Hagerman PJ; Hagerman RJ
    J Clin Psychiatry; 2009 Jun; 70(6):852-62. PubMed ID: 19422761
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Conversational characteristics of children with fragile X syndrome: tangential language.
    Sudhalter V; Belser RC
    Am J Ment Retard; 2001 Sep; 106(5):389-400. PubMed ID: 11531459
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Future of Fragile X Syndrome: CDC Stakeholder Meeting Summary.
    Riley C; Mailick M; Berry-Kravis E; Bolen J
    Pediatrics; 2017 Jun; 139(Suppl 3):S147-S152. PubMed ID: 28814536
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.
    McConkie-Rosell A; Finucane B; Cronister A; Abrams L; Bennett RL; Pettersen BJ
    J Genet Couns; 2005 Aug; 14(4):249-70. PubMed ID: 16047089
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Checklist assessments of FMR1 gene mutation phenotypes.
    Johnson VA
    J Cult Divers; 2008; 15(3):117-31. PubMed ID: 19025200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Conversational skills of individuals with fragile-X syndrome: a comparison with autism and Down syndrome.
    Ferrier LJ; Bashir AS; Meryash DL; Johnston J; Wolff P
    Dev Med Child Neurol; 1991 Sep; 33(9):776-88. PubMed ID: 1834506
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X Newborn Screening: Lessons Learned From a Multisite Screening Study.
    Bailey DB; Berry-Kravis E; Gane LW; Guarda S; Hagerman R; Powell CM; Tassone F; Wheeler A
    Pediatrics; 2017 Jun; 139(Suppl 3):S216-S225. PubMed ID: 28814542
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical practice guidelines for Fragile X syndrome].
    Clinical Genetics Group Of Medical Geneticist Branch Of Chinese Medical Doctor Association ; Clinical Genetics Group Of Medical Genetics Branch Of Chinese Medical Association ; Genetic Disease Prevention And Control Group Of Professional Committee For Birth Defect Prevention And Control Of Chinese Preventive Medicine Association ; Duan R; Li G; Xi H; Peng Y; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Nov; 39(11):1181-1186. PubMed ID: 36317200
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fragile X syndrome.
    Hayes EW; Matalon R
    Pediatrics; 2009 Aug; 124(2):790-2. PubMed ID: 19581265
    [No Abstract]   [Full Text] [Related]  

  • 16. The psychiatric presentation of fragile x: evolution of the diagnosis and treatment of the psychiatric comorbidities of fragile X syndrome.
    Tranfaglia MR
    Dev Neurosci; 2011; 33(5):337-48. PubMed ID: 21893938
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Social cognition in adolescent girls with fragile x syndrome.
    Turkstra LS; Abbeduto L; Meulenbroek P
    Am J Intellect Dev Disabil; 2014 Jul; 119(4):319-39. PubMed ID: 25007297
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aberrant behaviors of young boys with fragile X syndrome.
    Lachiewicz AM; Spiridigliozzi GA; Gullion CM; Ransford SN; Rao K
    Am J Ment Retard; 1994 Mar; 98(5):567-79. PubMed ID: 8192902
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X syndrome.
    Saldarriaga W; Tassone F; González-Teshima LY; Forero-Forero JV; Ayala-Zapata S; Hagerman R
    Colomb Med (Cali); 2014; 45(4):190-8. PubMed ID: 25767309
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
    Wang H; Zhu X; Gui B; Cheung WC; Shi M; Yang Z; Kwok KY; Lim R; Pietilä S; Zhu Y; Choy KW
    J Vis Exp; 2019 Sep; (151):. PubMed ID: 31566610
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.