Implementing expanded prenatal genetic testing: should parents have access to any and all fetal genetic information?

MJ Bayefsky, BE Berkman - The American journal of bioethics, 2022 - Taylor & Francis
Prenatal genetic testing is becoming available for an increasingly broad set of diseases, and
it is only a matter of time before parents can choose to test for hundreds, if not thousands, of …

Expanding use of cfDNA screening in pregnancy: current and emerging ethical, legal, and social issues

L Parham, M Michie, M Allyse - Current Genetic Medicine Reports, 2017 - Springer
Abstract Purpose of Review In 2011, screening platforms became available in the US that
detect and analyze fragments of cell-free placental DNA (cfDNA) in maternal blood serum …

Termination of pregnancy for foetal indication in the French context analysis of decision-making in a Multidisciplinary Centre For Prenatal Diagnosis

S Baumann, S Darquy, C Miry, N Duchange… - Journal of Gynecology …, 2021 - Elsevier
Abstract Objective In France, termination of pregnancy (TOP) for medical reasons is legal,
regardless of the term, after authorisation by a Multidisciplinary Centre for Prenatal …

Reproductive Technologies and Free Speech

SM Suter - Journal of Law, Medicine & Ethics, 2021 - cambridge.org
The Supreme Court and lower courts have not articulated a clear or consistent framework for
First Amendment analysis of speech restrictions in health care and with respect to abortion …

Clash of the Titans: Escalating Conflict Between Surrogacy Contract Provisions and the Recriminalization of Abortion

HL Berk - Journal of Women, Politics & Policy, 2024 - Taylor & Francis
What will the practice of surrogacy contracting look like in states where abortion is
significantly restricted or banned, and how will it impact the wider baby market? Using …

Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry

A Pietropolli, MV Capogna, R Cascella, C Germani… - Human Genomics, 2016 - Springer
Background The knowledge of the individual genetic “status” in the prenatal era is
particularly relevant in the case of positive family history for genetic diseases, in advanced …

[HTML][HTML] Konjenital anomali prenatal taramalarında bir belirteç olarak mirna profilinin belirlenmesi

Ş Balcı Fidancı - 2023 - acikerisim.mersin.edu.tr
ÖZET KONJENİTAL ANOMALİ PRENATAL TARAMALARINDA BİR BELİRTEÇ OLARAK
MİRNA PROFİLİNİN BELİRLENMESİ Genetik defekt, kromozomal anöploidi ve yapısal …

[PDF][PDF] Prenatal tanı yöntemi olarak fetal anöploidi taramasında serbest fetal DNA (cffDNA) kullanımı ve güncel yaklaşımlar

H Erbaba, G Pınar - J Clin Exp Invest www. jceionline. org Vol, 2015 - researchgate.net
Prenatal tanı invaziv ve non-invaziv test (NIPT) şeklinde yapılabilmektedir, ancak invaziv
yöntemler abortus, enfeksiyon gibi risklere sahip olduğundan tanılamada non-invaziv …

NIPT and Sex Selection: Genetic Counselors' Experience Counseling Patients Who Intend to Use NIPT as a Screening Tool for Non-medical Sex Selection

E Orr-Ferdinand - 2021 - search.proquest.com
Non-medical sex selection (NMSS) is the practice of using medical techniques to choose the
sex of offspring for social, economical, cultural, and/or personal reasons, a practice that …

The usage and current approaches of cell free fetal DNA (cffDNA) as a prenatal diagnostic method in fetal aneuploidy screening

H Erbaba, G Pınar - Journal of Clinical and Experimental …, 2015 - dergipark.org.tr
Prenatal tanı invaziv ve non-invaziv test (NIPT) şeklinde yapılabilmektedir, ancak invaziv
yöntemler abortus, enfeksiyon gibi risklere sahip olduğundan tanılamada non-invaziv …