1. A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]. (4th July 2021) Authors: Lei, Ya-Li; Liang, Yue-Mei; Cao, Qun; Sui, Hong; Li, Dong-Zhi Journal: Hemoglobin Issue: Volume 45:Number 4(2021) Page Start: 254 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>T. (4th May 2021) Authors: Tian, Qi; Lei, Ya-Li; Xu, Li-Li; Li, Dong-Zhi Journal: Hemoglobin Issue: Volume 45:Number 3(2021) Page Start: 210 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Foetal phenotype of ALG1-CDG caused by paternal uniparental disomy 16. (4th July 2021) Authors: Lei, Ya-Li; Zhen, Li; Xu, Li-Li; Yang, Yan-Dong; Li, Dong-Zhi Journal: Journal of obstetrics and gynaecology Issue: Volume 41:Number 5(2021) Page Start: 828 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C). (3rd September 2019) Authors: Lei, Ya-Li; Sui, Hong; Liu, Yu-Juan; Pan, Jun-Jun; Liu, Yan-Hui; Lou, Ji-Wu Journal: Hemoglobin Issue: Volume 43:Number 4/5(2019) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗