Do patients with sickle-cell anaemia (HbSS) experience more oral and maxillofacial pain and altered facial sensation than patients with haemoglobin SC (HbSC) disease
M.F. Kiernan, H. Ho, L. Cheng, T. Sato, Q. Naqvi, Z. Imran, R. AmosVolume:
40
Year:
2011
Language:
english
DOI:
10.1016/j.ijom.2011.07.654
File:
PDF, 103 KB
english, 2011