Handbook of Genetic Diagnostic Technologies in Reproductive Medicine: Improving Patient Success Rates and Infant Health

Description

This expanded new edition covers the range of the latest genetic diagnostic technologies being translated into practice internationally to improve routine IVF procedures for the benefit of patients. Cover Title Page Copyright Page Table of Contents Contributors Preface Chapter 1 The Brave New World of Genomics Chapter 2 Genetics at the Cell Level: The Human Cell Atlas Chapter 3 The Genetic Risk of a Couple Aiming to Conceive Chapter 4 Carrier Screening for Single-Gene Disorders Chapter 5 Meiotic Abnormalities in Infertile Males Chapter 6 Chromosomal Analysis of Sperm Chapter 7 Epigenetics in Sperm, Epigenetic Diagnostics, and Transgenerational Inheritance Chapter 8 Aneuploidy in Human Oocytes and Preimplantation Embryos Chapter 9 Epigenetics from Oocytes to Embryos Chapter 10 Embryo Kinetics and Aneuploidy Chapter 11 Preimplantation Genetic Testing of Aneuploidies (PGT-A) Chapter 12 Preimplantation Genetic Testing for Structural Rearrangements Chapter 13 Mosaicism in Preimplantation Embryos Chapter 14 Embryo Cell-Free DNA in the Culture Medium and Its Potential for Non-Invasive Aneuploidy Testing Chapter 15 Mitochondria and Embryo Viability Chapter 16 Preimplantation Genetic Diagnosis for Single Gene Disorders Chapter 17 Preimplantation Genetic Testing for Polygenic Disorders Chapter 18 Should Genome Editing Replace Embryo Selection Following PGT? Chapter 19 Molecular Diagnosis of Endometrial Receptivity Chapter 20 The Vaginal Microbiome Chapter 21 The Uterine Microbiota Chapter 22 Endometritis: New Times, New Opportunities Chapter 23 Decidualization Resistance: A New Condition Identified in Severe Preeclampsia Chapter 24 Advanced Cell Therapy for Asherman’s Syndrome Chapter 25 Differential Genetic Diagnosis between Leiomyoma and Leiomyosarcoma Chapter 26 Non-Invasive Prenatal Testing (NIPT) Chapter 27 Advances in Non-Invasive Diagnosis of Single-Gene Disorders and Fetal Exome Sequencing Chapter 28 Chromosome Abnormalities in Human Pregnancy Loss: A Review of Cytogenetic and Molecular Analyses Chapter 29 Products of Conception: Current Methodologies and Clinical Applications Chapter 30 Mother and Embryo Cross Communication during Conception Chapter 31 Perinatal and Pediatric Outcome of Pregnancies Following PGT-M/SR/A Chapter 32 Genetic Counseling in Assisted Reproductive Technology Index