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P284: Compound heterozygosity for loss-of-function variants in GDF1 provides a molecular diagnosis in a patient with heterotaxy syndrome
oleh: Vittoria Rossi, Xi Luo, Kristin Cardiel Nunez, Ruiyang Yi, Elizabeth Mizerik, Lauren Westerfield, Seema Lalani, Mir Reza Bekheirnia
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2023-01-01 |
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