Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients - Qin, Danqing; Du, Li; Wang, Jicheng; Yao, Cuize; Guo, Hao; Yuan, Tenglong; Liang, Jie; Yin, Aihua (Journal of international medical research, 2020)
Keywords: alpha-Thalassemia - diagnosis; alpha-Thalassemia - genetics; Asian Continental Ancestry Group - genetics; Blood diseases; Capillary electrophoresis; Case Report; Case reports; Genotype; Genotype & phenotype; Hematologic Tests; Hemoglobin; Hemoglobins, Abnormal - genetics; Humans; Compound heterozygosity; hemoglobin Broomhill; Sanger sequencing; Southeast Asian α-thalassemia deletion; capillary electrophoresis; hemoglobin variant