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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Short Communication

A Fetus with Hb Bart’s Disease Due to Maternal Uniparental Disomy for Chromosome 16

Patrick K.C. AuDepartment of Obstetrics & Gynaecology, Queen Mary Hospital, Hong Kong SAR, People’s Republic of China Correspondence[email protected]
,
Anita S.Y. KanDepartment of Obstetrics & Gynaecology, Queen Mary Hospital, Hong Kong SAR, People’s Republic of China ;Department of Obstetrics & Gynaecology, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Mary H.Y. TangDepartment of Obstetrics & Gynaecology, Queen Mary Hospital, Hong Kong SAR, People’s Republic of China ;Department of Obstetrics & Gynaecology, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Kwok Y. LeungDepartment of Obstetrics & Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, People’s Republic of China
,
Kelvin Y.K. ChanDepartment of Obstetrics & Gynaecology, Queen Mary Hospital, Hong Kong SAR, People’s Republic of China ;Department of Obstetrics & Gynaecology, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
,
Tommy W.F. TangDepartment of Obstetrics & Gynaecology, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
&
Elizabeth T. LauDepartment of Obstetrics & Gynaecology, Queen Mary Hospital, Hong Kong SAR, People’s Republic of China ;Department of Obstetrics & Gynaecology, The University of Hong Kong, Hong Kong SAR, People’s Republic of China
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Pages 66-69 | Received 13 Jul 2015, Accepted 07 Sep 2015, Published online: 16 Nov 2015

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Hui Wang, Caiqun Luo, Yang Liu, Shengli Li, Niping Jiang, Guanglin Zhang, Jiansheng Xie & Mei Zhong. (2018) UPD16 itself is not a cause of intrauterine growth restriction. Fetal and Pediatric Pathology 37:6, pages 452-464.
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Articles from other publishers (8)

Xia Li. 2023. Cases in Laboratory Genetics and Genomics (LGG) Practice. Cases in Laboratory Genetics and Genomics (LGG) Practice 65 81 .
Pui Wah Hui, Polly Pang & Mary H. Y. Tang. (2022) 20 years review of antenatal diagnosis of haemoglobin Bart's disease and treatment with intrauterine transfusion. Prenatal Diagnosis 42:9, pages 1155-1161.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 85 184 .
Li‐Li Xu, Ying‐Na Liu, Li Zhen & Dong‐Zhi Li. (2019) Germline mosaicism in an α‐thalassemia family: Incidental identification by prenatal ultrasound. Prenatal Diagnosis 39:12, pages 1166-1169.
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Shirley S. W. Cheng, Kelvin Y. K. Chan, Kelphen K. P. Leung, Patrick K. C. Au, Wai‐Keung Tam, Samuel K. M. Li, Ho‐Ming Luk, Anita S. Y. Kan, Brian H. Y. Chung, Ivan F. M. Lo & Mary H. Y. Tang. (2019) Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong. American Journal of Medical Genetics Part C: Seminars in Medical Genetics.
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Duantida Songdej, Christian Babbs & Douglas R. Higgs. (2017) An international registry of survivors with Hb Bart's hydrops fetalis syndrome. Blood 129:10, pages 1251-1259.
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Xuan Shang & Xiangmin Xu. (2017) Update in the genetics of thalassemia: What clinicians need to know. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 3-15.
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Greggory R. DeVore, Kareem Tabsh, Bardo Polanco, Gary Satou & Mark Sklansky. (2016) Fetal Heart Size. Journal of Ultrasound in Medicine 35:12, pages 2543-2562.
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