Genetics and Genomics of Recurrent Pregnancy Loss
- 28 September 2018
- book chapter
- book charpter
- Published by Elsevier BV
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Dynamic Association of NUP98 with the Human GenomePLoS Genetics, 2013
- Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriagePlacenta, 2013
- Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot studyMolecular Cytogenetics, 2012
- Atypical E2F Repressors and Activators Coordinate Placental DevelopmentDevelopmental Cell, 2012
- Insufficient maintenance DNA methylation is associated with abnormal embryonic developmentBMC Medicine, 2012
- Methylation Allelic Polymorphism (MAP) in Chorionic Gonadotropin β5 (CGB5) and Its Association with Pregnancy SuccessJournal of Clinical Endocrinology & Metabolism, 2011
- The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by α-T-catenin upregulationHuman Molecular Genetics, 2010
- Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conceptionMolecular Human Reproduction, 2009
- Mutations of the SYCP3 Gene in Women with Recurrent Pregnancy LossAmerican Journal of Human Genetics, 2009
- Allele-Specific Targeting of microRNAs to HLA-G and Risk of AsthmaAmerican Journal of Human Genetics, 2007