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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 6
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Short Communication

An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations

Helena H. L. LeeDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
Annisa S. L. MakDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
K. O. KouDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
C. F. PoonDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
W. S. WongDepartment of Clinical Pathology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
K. H. ChiuDepartment of Paediatrics, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China;
,
Patrick K. C. AuPrenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Kelvin Y. K. ChanPrenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Anita S. Y. KanPrenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Mary H. Y. TangPrenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
&
K. Y. LeungDepartment of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China; Correspondence[email protected]
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Pages 431-434 | Received 07 Oct 2016, Accepted 30 Oct 2016, Published online: 31 Mar 2017

Citations (10)

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Read on this site (2)

Hua Jiang, Fan Jiang, Jian Li, Fang Tang & Dong-Zhi Li. (2019) Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report. Hemoglobin 43:4-5, pages 292-295.
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Fan Jiang, Yan-Xia Qu, Gui-Lan Chen, Jian Li, Jian-Ying Zhou, Lian-Dong Zuo, Can Liao & Dong-Zhi Li. (2018) KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population. Hemoglobin 42:3, pages 161-165.
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Articles from other publishers (8)

Kritsada Singha, Nattiya Teawtrakul, Goonnapa Fucharoen & Supan Fucharoen. (2023) Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series. Journal of Clinical Pathology, pages jcp-2023-208945.
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Kun Yang, Weiye Nie, Qiuying Huang, Guiping Liao, Jian Xiao & Xiaolin Yin. (2023) Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations. Annals of Hematology 102:6, pages 1621-1624.
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Cristian Antonio Caria, Valeria Faà & Maria Serafina Ristaldi. (2022) Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis. Cells 11:19, pages 3069.
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Maeve Wells & Laurie Steiner. (2022) Epigenetic and Transcriptional Control of Erythropoiesis. Frontiers in Genetics 13.
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Tanu Tangsricharoen, Rungrote Natesirinilkul, Arunee Phusua, Kanda Fanhchaksai, Chupong Ittiwut, Wanna Chetruengchai, Monthana Juntharaniyom, Pimlak Charoenkwan, Vip Viprakasit, Chureerat Phokaew & Vorasuk Shotelersuk. (2021) Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review . British Journal of Haematology 194:3, pages 626-634.
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Linlin Xu, Dina Zhu, Yanxia Zhang, Guanxia Liang, Min Liang, Xiaofeng Wei, Xiaoqing Feng, Xuedong Wu & Xuan Shang. (2021) Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review. Frontiers in Genetics 12.
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Gloria Barbarani, Cristina Fugazza, John Strouboulis & Antonella E. Ronchi. (2019) The Pleiotropic Effects of GATA1 and KLF1 in Physiological Erythropoiesis and in Dyserythropoietic Disorders. Frontiers in Physiology 10.
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Kevin Gillinder, Graham Magor & Andrew Perkins. (2018) Variable serologic and other phenotypes due to KLF1 mutations. Transfusion 58:5, pages 1324-1325.
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