Is this a genesis in prenatal testing: Genomic knowledge, risk or benefit?

Genetic Testing and Molecular Biomarkers

Volumn 16, Issue 12, 2012, Pages 1347-1348

  Jahnke, Christine M ^a,b   Stark, Elizabeth ^a   Terry, Sharon F ^a   Bonhomme, Natasha ^a  

^a GENETIC ALLIANCE   (United States)

^b GEORGETOWN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; EDITORIAL; EPIGENETICS; FETUS DEVELOPMENT; FETUS KARYOTYPING; GENE MUTATION; GENETIC DISORDER; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETIC VARIABILITY; PRENATAL SCREENING; RISK BENEFIT ANALYSIS;

FEMALE; GENETIC COUNSELING; GENETIC TESTING; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; RISK FACTORS;

EID: 84869403351     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2012.1538     Document Type: Editorial

References (3)

1. de Jong A, Dondrop WJ, de Die-Smulders CEM, et al. (2010) Non-invasive prenatal testing: ethical issues explored. Eur J Hum Genet 18:272-277.
2. Hayden EC (2012) Fetal tests spur legal battle. Nature 486:454.
3. Kitzman JQ, Snder MW, Ventura M, et al. (2012) Noninvasive whole-genome sequencing of a human fetus. Sci Transl Med 4:137ra76.