Prenatal genetics

877 - Copy Number Variations of 1q21.1 Are Clinically Associated with Fetal Structural Neurologic Abnormalities  

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868 - BearGenes: An App to Increase Accessibility to Reliable Clinical Genetics Information

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883 - Recommendations Versus Practice Patterns:  The Uptake of Chromosomal Microarray Testing in Prenatal Patients With Structural Ultrasound Abnormalities
893 - Prenatal Diagnosis of severe manifestations of Kagami-Ogata Syndrome caused by paternal unipaternal disomy 14 
894 - Observations of Non-Ashkenazi Jewish (AJ) Individuals Testing Positive for AJ Disorders
895 - Microarray Detection of Mosaicism in Prenatal and POC Specimens:  More Complexity with Better Technology
897 - Maternal Chimerism as a Cause of Confounded Gender Reporting and Gender Discordance During cfDNA Screening
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