SERN-SERGG-2014

Carol Saunders, PhD, FACMG — Diagnosing the Previously Undiagnosable through Genomic Medicine (SERN/SERGG 2014)

David Everman, MD — The Clinical and Molecular Complexity of Split-hand/foot Malformation (SERN/SERGG 2014)

Lucas Bronicki, PhD — Integrating Next-Generation Sequencing and Microarray Technologies for a More Comprehensive Analysis in Autism Patients (SERN/SERGG 2014)

Pamela Arn, MD — Genetics Clinic in the 21st Century (SERN/SERGG 2014)

Olaf Bodamer, MD, PhD, FCCMG — Newborn Screening in the Genomic Era (SERN/SERGG 2014)

Eva Morava, MD, PhD — Defining Manibi Deficiency (SERN/SERGG 2014)

Joan Scott, CGC, MS — Updates from the Genetic Services Branch, MCHB (SERN/SERGG 2014)

Updates from the Genetic Services Branch, MCHB.

Beth Tarini, MD, MS — The Challenge of Integrating Genetics Into Primary Care Pediatrics – Can We Get the Camel Through the Eye of the Needle? (SERN/SERGG 2014)

Stephen Hooper, PhD — The LEND Network: Translational Possibilities (SERN/SERGG 2014)

Michael Watson, PhD, FACMG — National Coordinating Center (NCC) Update (SERN/SERGG 2014)

Dr. Watson provides an update on NCC activities.

Hans Andersson, MD — Phenylalanine Hydroxylase Deficiency ACMG Practice Guidelines (SERN/SERGG 2014)

Janet Hess, DrPH, MPH, CHES — FloridaHATS: Building Bridges from Pediatric to Adult Care (SERN/SERGG 2014)

Dr. Janet Hess presents, FloridaHATS: Building Bridges from Pediatric to Adult Care.

Amy Cunningham, RD, LDN, MS — Recommendations for the Nutrition Management of Phenylalanine Hydroxylase Deficiency (SERN/SERGG 2014)

Amy Cunningham talks about newly released SERC/GMDI PKU Nutrition Management Guidelines.