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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 5
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Short Communication

Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion

Xin YangPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;
,
Jin-Mei YanPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;
,
Jian LiPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;
,
Xing-Mei XiePrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;
,
Jian-Ying ZhouPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;
,
Yan LiGuangzhou Cord Blood Bank, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of ChinaCorrespondence[email protected]; Dr Yan Li [email protected]
&
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China; Correspondence[email protected]; Dr Yan Li [email protected]
 show all
Pages 353-355 | Received 29 Jun 2016, Accepted 20 Aug 2016, Published online: 30 Sep 2016

References

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  • Durmaz AA, Akin H, Ekmekci AY, et al. A severe αthalassemia case compound heterozygous for Hb Adana in α1 gene and 20.5 kb double gene deletion. J Pediatr Hematol Oncol. 2009;31(8):592–594.
  • Henderson S, Pitman M, McCarthy J, et al. Molecular prenatal diagnosis of Hb H hydrops fetalis caused by Haemoglobin Adana and the implications to antenatal screening for α-thalassaemia. Prenat Diagn. 2008;28:859–861.
  • Alauddin H, Jaapar NA, Azma RZ, et al. A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay families. Hemoglobin. 2014;38(4):277–281.

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