Session Datesort descending
1/8/25: Experiences of Predictive Genetic Testing in Inherited Motor Neuron Disease 01/08/2025 - 4:00pm to 5:00pm CST
1/15/25: Neonatal Progeroid Syndrome: Lipodystrophy; Craniofacial, Dental, Ocular & Digital Anomalies; and Short Stature & Incidental Findings in Panel Testing for Sensorineural Hearing Loss 01/15/2025 - 4:00pm to 5:00pm CST
1/29/25: Undiagnosed Disease Program Case Review 01/29/2025 - 4:00pm to 5:00pm CST
2/5/25: Short Rib Polydactyly Syndrome (SRPS) – a Challenging Recurrence & Navigating the Diagnostic Process from Prenatal to Newborn 02/05/2025 - 4:00pm to 5:00pm CST
2/12/25: Genetic Predictors of Monogenic Etiology in Familial Short Stature (FSS) 02/12/2025 - 4:00pm to 5:00pm CST
2/19/25: Navigating a Case of Mixed Dyslipidemia: Counseling Considerations and A Rare Find & Counseling Considerations and Cascade Testing in a Family with Hereditary Cancer 02/19/2025 - 4:00pm to 5:00pm CST
3/5/25: Where Did This Come From? : A Question of Paternity in a Rare Case of COL11A1 Related Syndrome & AD and Me: Making a Case for a Preventative Model of Care 03/05/2025 - 4:00pm to 5:00pm CST
3/12/25: Eighteen‐Month Real‐World Experience Using Mavacamten for Treatment of Obstructive Hypertrophic Cardiomyopathy in a Racially Diverse Population 03/12/2025 - 4:00pm to 5:00pm CDT
4/2/25: When is the Picture Complete? The Process of Characterizing Chromosomal Abnormalities 04/02/2025 - 4:00pm to 5:00pm CDT
4/9/25: The Multigenerational Impact of Long QT Syndrome: A Gitxsan Perspective 04/09/2025 - 4:00pm to 5:00pm CDT

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