Non-Sickle Cell Structural Hemoglobinopathies
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-99-8933-1_22
Reference13 articles.
1. Matos JF, Dusse LMS, Borges KBG, et al. A new index to discriminate between iron deficiency anemia and thalassemia trait. Rev Bras Hematol Hemoter. 2016;38(3):214–9. https://doi.org/10.1016/j.bjhh.2016.05.011.
2. Powars DR, Hiti A, Ramicone E, Johnson C, Chan L. Outcome in hemoglobin SC disease: a four-decade observational study of clinical, hematologic, and genetic factors. Am J Hematol. 2002;70(3):206–15.
3. Olson JF, Ware RE, Schultz WH, Kinney TR. Hemoglobin C disease in infancy and childhood. J Pediatr. 1994 Nov;125(5 Pt 1):745–7.
4. Rezende PV, Santos MV, Campos GF, Vieira LLM, Souza MB, Belisário AR, Silva CM, Viana MB. Clinical and hematological profile in a newborn cohort with hemoglobin SC. J Pediatr. 2018;94(6):666–72.
5. Chmel H, Bertles JF. Hemoglobin S/C disease in a pregnant woman with crisis and fat embolization syndrome. Am J Med. 1975;58(4):563–6.
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