APA

Kanathezhath B., Hazard F. K., Guo H., Kidd J., Azimi M., Kuypers F. A., Vichinsky E. P. & Lal A. (20100126). Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. : Pediatric blood & cancer.

Chicago

Kanathezhath B, Hazard F K, Guo H, Kidd J, Azimi M, Kuypers F A, Vichinsky E P and Lal A. 20100126. Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. : Pediatric blood & cancer.

Harvard

Kanathezhath B., Hazard F. K., Guo H., Kidd J., Azimi M., Kuypers F. A., Vichinsky E. P. and Lal A. (20100126). Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. : Pediatric blood & cancer.

MLA

Kanathezhath B, Hazard F K, Guo H, Kidd J, Azimi M, Kuypers F A, Vichinsky E P and Lal A. Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. : Pediatric blood & cancer. 20100126.