Filtre: Konu
Toplam kayıt 1, listelenen: 1-5
8p23.1 Deletion Syndrome (1) |
Absence Seizure (1) |
Genomic Copy Number Variation (1) |
MIR597 (1) |
XKR6 (1) |
8p23.1 Deletion Syndrome (1) |
Absence Seizure (1) |
Genomic Copy Number Variation (1) |
MIR597 (1) |
XKR6 (1) |