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Pediatric Hematology and Oncology Volume 35, 2018 - Issue 7-8
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Fetal-onset congenital dyserythropoietic anemia type 1 due to CDAN1 mutations presenting as hydrops fetalis

Sha LiuDepartment of Pediatric Hematology-Oncology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China; View further author information
, BS,
Ying-Na LiuDepartment of Obstetrics and Gynecology, Shenzhen Hospital of Southern Medical University, Shenzhen, China; View further author information
, MS,
Li ZhenPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaView further author information
, PhD &
Dong-Zhi LiPrenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaCorrespondence[email protected]
View further author information
, PhD
Pages 447-450 | Received 17 Sep 2018, Accepted 30 Nov 2018, Published online: 20 Feb 2019

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Read on this site (1)

Esther Dempsey, Tessa Homfray, John M Simpson, Steve Jeffery, Sahar Mansour & Pia Ostergaard. (2020) Fetal hydrops – a review and a clinical approach to identifying the cause. Expert Opinion on Orphan Drugs 8:2-3, pages 51-66.
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Articles from other publishers (2)

Amy E. Geddis, Meera Srikanthan & Katie Bergstrom. 2021. Neonatal Hematology. Neonatal Hematology 43 61 .
Abed Abu‐Quider, Mahdi Asleh, Hanna Shalev, Yariv Fruchtman, Meriam Ben‐Harosh, Guy Beck & Josef Kapelushnik. (2020) Treatment of transfusion‐dependent congenital dyserythropoietic anemia Type I patients with pegylated interferon alpha‐2a. European Journal of Haematology 105:2, pages 216-222.
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