P284: Compound heterozygosity for loss-of-function variants in GDF1 provides a molecular diagnosis in a patient with heterotaxy syndrome
Vittoria Rossi(Texas Children's Hospital), Mir Reza Bekheirnia(Baylor College of Medicine), Kristin Cardiel Nunez(Mayo Clinic in Arizona), Lauren Westerfield(Texas Children's Hospital), Ruiyang Yi(Texas Children's Hospital), Elizabeth Mizerik(Baylor College of Medicine), Xi Luo(Chinese Academy of Sciences), Seema R. Lalani(Baylor College of Medicine)
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