Information Journal Paper
APA:
Copy. (2019). Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: Matching with osmotic fragility test and presence of spherocyte. ORPHANET JOURNAL OF RARE DISEASES, 14(1), 114-114. SID. https://sid.ir/paper/981220/en
Vancouver:
Copy. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: Matching with osmotic fragility test and presence of spherocyte. ORPHANET JOURNAL OF RARE DISEASES[Internet]. 2019;14(1):114-114. Available from: https://sid.ir/paper/981220/en
IEEE:
Copy, “Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: Matching with osmotic fragility test and presence of spherocyte,” ORPHANET JOURNAL OF RARE DISEASES, vol. 14, no. 1, pp. 114–114, 2019, [Online]. Available: https://sid.ir/paper/981220/en