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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

Citations (7)

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Read on this site (3)

Shao-Min Wu, Su-Ran Huang, Chan Li, Gui-Lan Chen & Dong-Zhi Li. (2022) Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report. Hemoglobin 46:6, pages 341-343.
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Xiao-Hong He, Rui Zhang, Guang-Xing Mai, Li-Rong Ren & Dong-Zhi Li. (2018) First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene. Hemoglobin 42:5-6, pages 344-346.
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Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li. (2017) Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 41:4-6, pages 293-296.
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Articles from other publishers (4)

Ashutosh Lal & Elliott Vichinsky. (2023) The Clinical Phenotypes of Alpha Thalassemia. Hematology/Oncology Clinics of North America 37:2, pages 327-339.
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Li Du, Xiuqin Bao, Wei He, Danqing Qin, Jicheng Wang, Ying Xiong, Xiaomei Shi, Hongke Ding, Cuize Yao & Jing Wu. (2021) Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden ( HBA2 :c.178G>C) and Hb Quong Sze ( HBA2 :c.377T>C) . Journal of International Medical Research 49:7, pages 030006052110314.
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Prashant Sharma, Reena Das, Alka Rani Khadwal, Indrani Karmakar, Jasbir Kaur Hira & Sanjeev Chhabra. (2020) HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches. Pediatric Blood & Cancer 67:4.
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Gisele A. Pedroso, Elza M. Kimura, Magnun N.N. Santos, Dulcinéia M. Albuquerque, Danaê Malimpensa, Susan E. Jorge, Monica P.A. Verissimo, Fernando F. Costa & Maria F. Sonati. (2018) Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child. Pediatric Blood & Cancer 65:12, pages e27413.
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