论文信息 - Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature - 字舞流文

Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature

M. I. Melaragno | C. B. de Mello | F. T. Bellucco | V. A. Meloni | M. Melaragno | Fernanda T Bellucco