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 *

206 related articles for article (PubMed ID: 8247721)

  • 1. [Ethical and psychological aspects of screening tests for children].
    Dehlholm G; Hansen D
    Nord Med; 1993; 108(11):297-9. PubMed ID: 8247721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Psychosocial consequences of screening programs in children].
    Hansen D; Dehlholm B
    Nord Med; 1992; 107(11):280-2. PubMed ID: 1448343
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic screening: programs, principles, and research--thirty years later. Reviewing the recommendations of the Committee for the Study of Inborn Errors of Metabolism (SIEM).
    Simopoulos AP;
    Public Health Genomics; 2009; 12(2):105-11. PubMed ID: 19039254
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Predictive medicine--ethical and social aspects of genetic diagnosis].
    Bayertz K
    Geburtshilfe Frauenheilkd; 1996 Apr; 56(4):M55-7. PubMed ID: 8682278
    [No Abstract]   [Full Text] [Related]  

  • 5. [Ethical aspects of programs for genetic screening premarital diagnosis and prenatal diagnosis of hereditary diseases].
    Lisker R
    Rev Invest Clin; 1980; 32(1):1-5. PubMed ID: 7414137
    [No Abstract]   [Full Text] [Related]  

  • 6. The psychological impact of genetic testing on parents.
    Dinc L; Terzioglu F
    J Clin Nurs; 2006 Jan; 15(1):45-51. PubMed ID: 16390523
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.
    Bailey DB; Skinner D; Davis AM; Whitmarsh I; Powell C
    Pediatrics; 2008 Mar; 121(3):e693-704. PubMed ID: 18310190
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expanded newborn screening for biochemical disorders: the effect of a false-positive result.
    Gurian EA; Kinnamon DD; Henry JJ; Waisbren SE
    Pediatrics; 2006 Jun; 117(6):1915-21. PubMed ID: 16740831
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Examination of long-lasting parental concern after false-positive results of neonatal hearing screening.
    van der Ploeg CP; Lanting CI; Kauffman-de Boer MA; Uilenburg NN; de Ridder-Sluiter JG; Verkerk PH
    Arch Dis Child; 2008 Jun; 93(6):508-11. PubMed ID: 18218661
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predictive genetic testing in minors for adult-onset genetic diseases.
    Borry P; Goffin T; Nys H; Dierickx K
    Mt Sinai J Med; 2008; 75(3):287-96. PubMed ID: 18704981
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The clinical aspects of newborn screening: importance of newborn screening follow-up.
    James PM; Levy HL
    Ment Retard Dev Disabil Res Rev; 2006; 12(4):246-54. PubMed ID: 17183568
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic screening and testing in Canada: a model duty of care.
    Sharpe NF
    Health Law J; 1996; 4():119-34. PubMed ID: 10569885
    [No Abstract]   [Full Text] [Related]  

  • 13. Parental tolerance of false-positive newborn screening results.
    Prosser LA; Ladapo JA; Rusinak D; Waisbren SE
    Arch Pediatr Adolesc Med; 2008 Sep; 162(9):870-6. PubMed ID: 18762606
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Family pediatrics: report of the Task Force on the Family.
    Schor EL;
    Pediatrics; 2003 Jun; 111(6 Pt 2):1541-71. PubMed ID: 12777595
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cystic fibrosis newborn screening: impact of early screening results on parenting stress.
    Baroni MA; Anderson YE; Mischler E
    Pediatr Nurs; 1997; 23(2):143-51. PubMed ID: 9165929
    [TBL] [Abstract][Full Text] [Related]  

  • 16. State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results.
    Tarini BA; Christakis DA; Welch HG
    Pediatrics; 2006 Aug; 118(2):448-56. PubMed ID: 16882794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening pregnancies at risk for single gene disorders.
    Kelly TE
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():181-2. PubMed ID: 11400764
    [No Abstract]   [Full Text] [Related]  

  • 18. Integration of new genetic diseases into statewide newborn screening: New England experience.
    Comeau AM; Larson C; Eaton RB
    Am J Med Genet C Semin Med Genet; 2004 Feb; 125C(1):35-41. PubMed ID: 14755432
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Strategies and logistical requirements for efficient testing in genetic disease.
    Jackson-Cook C; Pandya A
    Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Advisory committee on heritable disorders and genetic diseases in newborns and children.
    Howell RR;
    Ment Retard Dev Disabil Res Rev; 2006; 12(4):313-5. PubMed ID: 17183571
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.