Nr.
Eintrag
1
Huys, Isabelle ; Van Overwalle, Geertrui ; Matthijs, Gert :Gene and genetic diagnostic method patent claims: a comparison under current European and US patent law.
2
Raspberry, Kelly ; Skinner, Debra :Enacting genetic responsibility: experiences of mothers who carry the fragile X gene.
3
Skinner, Debra et al.: Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.
4
Dye, Danielle E. et al.: The disclosure of genetic information: a human research ethics perspective
5
Bailey, Donald B. et al.: Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues
6
Delatycki, Martin B. :Population screening for reproductive risk for single gene disorders in Australia: now and the future.
7
Metcalfe, Sylvia et al.: A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study
8
Ross, Lainie Friedman ; Acharya, Kruti :Policy considerations in designing a fragile X population screening program.
9
Anido, Aimee ; Carlson, Lisa M. ; Sherman, Stephanie L. :Attitudes toward fragile X mutation carrier testing from women identified in a general population survey
10
de Silva, Rajith :Diagnostic DNA testing and consent
11
Pence, Gregory E. :Are genetic abortions eugenic?
12
Whitmarsh, Ian et al.: A place for genetic uncertainty: parents valuing an unknown in the meaning of disease
13
Fanos, Joanna H. ; Spangner, Kerstin A. ; Musci, Thomas J. :Attitudes toward prenatal screening and testing for Fragile X
14
Guzauskas, Gregory F. ; Lebel, Robert Roger :The duty to re-contact for newly appreciated risk factors: fragile X premutation
15
Hiraki, Susan et al.: Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children
16
American College of Medical Genetics: American College of Medical Genetics [policy statement on] fragile X syndrome : diagnostik and carrier testing
17
Schinzel, Albert A. :Indikation und Durchführung genetischer Diagnostik bei geistiger Behinderung unter besonderer Berücksichtigung des fragilen X- und des Down-Syndroms
18
Bernard, Lynn E. et al.: Duty to re-contact: a study of families at risk for Fragile X.
19
de Vries, Bert B.A. et al.: Dilemmas in counselling females with the fragile X syndrome.
20
Génétique et droits de l'homme
