A rare pair in one patient - Bernard-Soulier syndrome unraveled by 22q11.2 microdeletion syndrome

Gita Tauriņa, Daiga Mūrmane, Irēna Voitoviča, Sergejs Ņikuļšins, Ieva Mičule

Research output: Contribution to journal › Meeting Abstract › peer-review

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Biochemistry, Genetics and Molecular Biology