Prenatal genetics

908 - Identification of a Maternal Xp22.31 Deletion by Non-Invasive Prenatal Screening in the Setting of Clinical Suspicion for X-Linked Ichthyosis

Previous Eposter
907 - Prenatal Diagnosis of Inverted Duplication Deletion 8p Syndrome: 2 Case Reports and Review

Next Eposters
909 - Biallelic SCN5A Variants Cause Prenatal Onset of Complex Cardiac Arrhythmias
910 - Recurrent Hydatidiform Mole Associated with a Homozygous NLRP7 Variant
911 - Avoiding Unnecessary Trade-Offs: Clinical Experience for a Noninvasive Prenatal Screen with Both Low No-Call Rate and High Accuracy
914 - Beyond Insurance Billing – How Can ICD10 codes help direct noninvasive prenatal testing (NIPT) practice guidelines?
918 - MaterniT® 21 PLUS Performance in Lower Fetal Fraction Samples
919 - Recurrence of a Novel COL1A1 Variant in Subsequent Pregnancies with a Severe Osteogenesis Imperfecta Phenotype
922 - Leveraging Whole Genome Sequencing in Noninvasive Prenatal Screening: A Case of Prader-Willi Syndrome Due to Uniparental Disomy  
923 - Medical Genetics and Genomics Education During Maternal-Fetal Medicine Training: Bridging the Gap
928 - Presence of Y Chromosome Sequences in Maternal DNA Can Cause Incorrect Fetal Sex Determination in Non-Invasive Prenatal Testing
933 - The Utility of Re-testing Failed Noninvasive Prenatal Screening Samples Due to Low Fetal Fraction