Prenatal genetics

897 - Maternal Chimerism as a Cause of Confounded Gender Reporting and Gender Discordance During cfDNA Screening

Previous Eposter
895 - Microarray Detection of Mosaicism in Prenatal and POC Specimens:  More Complexity with Better Technology

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905 - Prenatal diagnosis of a 22q11.2 duplication in patient with previous child with 22q11.2 deletion syndrome
906 - Fetal Fraction in Non-Invasive Prenatal Testing is an Independent Risk Factor for Triploidy, Trisomy 18 and Trisomy 13
907 - Prenatal Diagnosis of Inverted Duplication Deletion 8p Syndrome: 2 Case Reports and Review
908 - Identification of a Maternal Xp22.31 Deletion by Non-Invasive Prenatal Screening in the Setting of Clinical Suspicion for X-Linked Ichthyosis
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