Preimplantation Genetic Diagnosis for Mendelian Conditions.

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Last Posted: Sep 09, 2017

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• Preimplantation Genetic Diagnosis for Mendelian Conditions.  
  Dolan Siobhan M et al. JAMA 2017 Sep (9) 859-860
• Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome.  
  Kou K O et al. Hong Kong medical journal = Xianggang yi xue za zhi 2016 Jun 22(3) 223-30
• Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.  
  Dheedene Annelies et al. Prenatal diagnosis 2016 Aug 36(8) 699-707
• No. 261-Prenatal Screening for Fetal Aneuploidy in Singleton Pregnancies.  
  Chitayat David et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2017 Sep 39(9) e380-e394
• No. 262-Prenatal Screening for and Diagnosis of Aneuploidy in Twin Pregnancies.  
  Audibert François et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2017 Sep 39(9) e347-e361
• No. 348-Joint SOGC-CCMG Guideline: Update on Prenatal Screening for Fetal Aneuploidy, Fetal Anomalies, and Adverse Pregnancy Outcomes.  
  Audibert Francois et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2017 Sep 39(9) 805-817
• Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping.  
  Vermeulen Carlo et al. American journal of human genetics 2017 Aug
• Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.  
  Neofytou Maria C et al. PloS one 2017 12(2) e0171319
• Supporting Women's Autonomy in Prenatal Testing.  
  Johnston Josephine et al. The New England journal of medicine 2017 Aug 377(6) 505-507
• The SEeMORE strategy: single-tube electrophoresis analysis-based genotyping to detect monogenic diseases rapidly and effectively from conception until birth.  
  Cariati Federica et al. Clinical chemistry and laboratory medicine 2017 Aug
• Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.  
  Chen Ying et al. Prenatal diagnosis 2016 Dec 36(13) 1233-1241
• Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies.  
  De Groote Katya et al. Prenatal diagnosis 2017 Jul
• Physician liability and non-invasive prenatal testing.  
  Toews Maeghan et al. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC 2014 Oct 36(10) 907-914
• Finding Middle Ground in Constructing a Clinically Useful Expanded Carrier Screening Panel.  
  Stevens Blair et al. Obstetrics and gynecology 2017 Jul
• Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing.  
  Horn Ruth et al. Prenatal diagnosis 2017 Jul
• Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies.  
  Lilley Margaret et al. Prenatal diagnosis 2017 Jul

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