Skip to main content
Fig. 4 | BMC Medical Genetics

Fig. 4

From: Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

Fig. 4

Hematological parameter analysis of heterozygotes of Chinese Gγ (Aγδβ)0 thalassemia, SEA-HPFH, Taiwanese deletion, and Italian nd-HPFH. Comparisons of hemoglobin (Hb) (a), mean corpuscular volume (MCV) (b), mean corpuscular hemoglobin (c), hemoglobin A2 (HbA2) (d), and fetal hemoglobin (HbF) (e) levels of those four types of δβ-thalassemia/HPFH with or without coinherited α0-thalassaemia (southeast Asian type deletion). Mean ± standard deviation (SD) isused to describe hematological parameters. A p-value of less than 0.05 showing significant differences: **p < 0.01; *p < 0.05

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us