REFERENCES
- Hsieh M, Tisdale J, Rodgers, G. Hemolytic anemia: thalassemias and sickle cell disorders. In: Rodgers G, Young N, Eds. Bethesda Handbook of Clinical Hematology. Philadelphia: Lippincott Williams & Wilkins. 2009:39–40.
- Bunn HF. Hemoglobins: normal and abnormal. In: Nathan DG, Orkin SH, Eds. Nathan and Oski’s: Hematology of Infancy and Childhood. Philadelphia: Saunders Elsevier. 2009:939–940.
- Benson JM, Therrell BL Jr. History and current status of newborn screening for hemoglobinopathies. Semin Perinatol. 2010;34(2):134–144.
- Tennessee Department of Health. Newborn screening: department of health: Tennessee government (http://health.state.tn.us/nbs/index.htm). Published 2010 (accessed January 10 2012).
- Smith EW, Krevans JR. Clinical manifestations of Hemoglobin C disorders. Bull Johns Hopkins Hosp. 1959;104(1):17–43.
- Redetzki JE, Bickers JN, Samuels MS. Homozygous Hemoglobin C disease: clinical review of fifteen patients. Southern Med J. 1968;61(3):238–242.
- Oslon JR, Ware RE, Schultz WH, Kinney TR. Hemoglobinc C disease in infancy and childhood. J Pediatr. 1994;125(5 Pt 1):745–747.
- Reinsch C. Smoothing by spline functions. Numerische Methematik.1967;177–183.
- World Health Organization child growth standards based on length/height, weight, and age. Acta Paediatr Suppl. 2006;450:76–85.
- Kuczmarski R, Ogden C, Guo S, . Centers for Disease Control and Prevention growth charts for the United States: methods and development. Vital Health Stat. 2002;11(246):1–203.
- Brugnara C. Reference values in infancy and childhood. In: Nathan DG, Orkin SH, Eds. Nathan and Oski’s: Hematology of Infancy and Childhood. Philadelphia: Saunders Elsevier. 2009:1774–1775.
- Minnichi V, Hill RJ, Khuri PD, Anderson ME. Hemoglobin Hope: a β chain variant. Blood. 1965;25:830–838.
- Baglioni C. The fusion of two peptide chains in Hemoglobin Lepore and its interpretation as a genetic deletion. Proc Natl Acad Sci USA. 1962;48:1880-1886.
- Quattrin N, Ventruto V. Hemoglobin Lepore: its significance for thalassemia and clinical manifestations. Blut. 1974;28(2):326–336.
- Higgs DR, Clegg JB, Wood WG, Weatherall DJ. Gγβ+ Type of hereditary persistence of fetal haemoglobin in association with Hb C. J Med Genet. 1979;16(4):288–295.
- Rodrigues de SL, Kimura EM, Albuquerque DM, . Hb Osu-Christiansborg [β52(D3)Asp→Asn]: a de novo mutation in Brazil. Hemoglobin. 2004;28(1):65–68.
- Pearson HA, Spencer RP, Cornelius EA. Functional asplenia in sickle cell anemia. N Engl J Med. 1969;281(17):923–926.