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A comparison of attitudes towards prenatal diagnosis and pre-implantation genetic diagnosis [PDF]
, 2010 Technological advances in prenatal screening and diagnosis mean that it is now possible to test for a wide range of congenital conditions (Hewison et al., 2007).
Miller, Chloe Louise
core +7 more sources
Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten-Year Single-Centre Experience. [PDF]
HaemophiliaABSTRACT Introduction Preimplantation genetic testing for monogenic diseases (PGT‐M) is a reproductive option for couples at high risk of transmitting inherited disorders. We report a ten‐year single‐centre PGT‐M experience in families at risk of hemophilia.
Mortarino M +6 more
europepmc +2 more sources
Preimplantation genetic diagnosis [PDF]
International Journal of Gynecology & Obstetrics, 2003 Preimplantation genetic diagnosis (PGD) is an exciting new approach for the prevention of transmission of genetic disorders between generations. The use of genetically screened, healthy embryos to establish a pregnancy avoids the need for termination of an affected pregnancy, a procedure which can be traumatic physically and emotionally for potential ...
G-L, Zhuang, J, Deng, D, Zhang
openaire +2 more sources
A ‘healthy baby’: The double imperative of preimplantation genetic diagnosis [PDF]
, 2010 This is the author's accepted manuscript. The final published article is available from the link below. Copyright @ 2010 The Authors.This article reports from a study exploring the social processes, meanings and institutions that frame and produce ...
Williams, C +3 more
core +1 more source
Journal of Human Reproductive Sciences, 2021 Preimplantation genetic testing (PGT) for monogenic disorders and assisted reproductive technology have evolved and progressed in tandem. PGT started with single-cell polymerase chain reaction (PCR) followed by fluorescent in situ hybridisation for a ...
Firuza R Parikh +7 more
doaj +1 more source
Attitudes toward prenatal diagnosis and termination of pregnancy in Saudi Arabia [PDF]
, 2004 INTRODUCTION: Advances in molecular biology will soon make it possible to offer parents prenatal testing for a large number of different genetic disorders.
Alsulaiman, Ayman
core +7 more sources
Social welfare, genetic welfare? Boundary-work in the IVF/PGD clinic [PDF]
, 2006 Copyright @ 2006 Elsevier Ltd. All rights reserved.Through the lens of the ‘welfare of the child’ assessment, this paper explores how staff working in the area of in vitro fertilisation and preimplantation genetic diagnosis (IVF/PGD) balance reflexive ...
Williams, C +10 more
core +1 more source
Frontiers in Physiology, 2022 Objective: To determine if the application of time-lapse incubation and monitoring can be beneficial to clinical outcomes in assisted reproductive technology.Methods: A total of 600 patients were equally randomized to three groups, namely, conventional ...
Yu-han Guo +19 more
doaj +1 more source
A Case of Enlarged Intracranial Translucency in a Fetus with Blake’s Pouch Cyst
Case Reports in Obstetrics and Gynecology, 2014 The intracranial translucency (IT) is a recently introduced marker of open spina bifida (OSB). In this study, we describe a case of a fetus affected by Blake’s pouch cyst which showed alterations of BS/BSOB ratio at the first trimester screening.
Ambra Iuculano +3 more
doaj +1 more source
Frontiers in Genetics, 2019 Preimplantation genetic testing for the monogenic disorder (PGT-M) spinal muscular atrophy (SMA) is significantly improved by supplementation of SMN1 deletion detection with marker-based linkage analysis. To expand the availability of informative markers
Mingjue Zhao +8 more
doaj +1 more source