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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 18, 2019
Chromosomal microarray analysis in pregnancies at risk for a molecular disorderDong-Zhi Li, Hai-Shen Tang
Hemoglobin|May 29, 2023
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case ReportsHai-Shen Tang, Yi Xiong, Dong-Zhi Li
Hemoglobin|June 12, 2012
Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] compromises neonatal screening for α-thalassemia with the Sebia Capillarys2 electrophoresis systemYin-Sheng Zhai, Hai-Shen Tang, Dong-Zhi Li
Hemoglobin|March 9, 2013
Codon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) causing nondeletional α-thalassemia in a Chinese familyCan Liao, Hai-Shen Tang, Ru Li, et al.
Hemoglobin|May 9, 2018
δ-Thalassemia with Complete Absence of Hb A<sub>2</sub> in a Chinese FamilyHai-Shen Tang, De-Gang Wang, Lv-Yin Huang, et al.
Hemoglobin|March 22, 2012
A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemiaYin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou, et al.
Hemoglobin|January 17, 2012
A novel α-thalassemia frameshift mutation: codon 8 (-C)Hai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin|November 16, 2013
Newborn screening for Hb H disease by determination of Hb Bart's using the Sebia capillary electrophoresis system in southern ChinaCan Liao, Jian-Ying Zhou, Xing-Mei Xie, et al.
Hemoglobin|January 14, 2012
Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis systemHai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 26, 2019
Can cell-free DNA testing be used in pregnancies with isolated fetal omphalocele? Preliminary evidence from cytogenetic results of prenatal casesLi-Li Xu, Li Zhen, Ji-Wu Lou, et al.
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