Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions - Wang, Yunan; Xiong, Ying; Liu, Chang; Lu, Jian; Wang, Jicheng; Qin, DanQing; Liu, Ling; Wu, Jing; Zhao, Xin; Fang, Liyuan; Du, Li; Yin, Aihua (Journal of international medical research, 2021)
Keywords: alpha-Globins - genetics; alpha-Thalassemia - diagnosis; alpha-Thalassemia - genetics; Blood diseases; Case Report; China; Edema; Female; Gene Deletion; Hemoglobin; Hemoglobins, Abnormal; Humans; Hydrops Fetalis - diagnosis; Hydrops Fetalis - genetics; Multigene Family; Mutation; Pregnancy; Prenatal Diagnosis; China; α-thalassaemia; Haemoglobin Bart’s hydrops; SEA deletion; SNP array; novel deletions; multiplex ligation-dependent probe amplification